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Suture Anchors

Suture Anchors are small devices used to attach soft tissues, such as tendons or ligaments, to bone.
They are commonly used in orthopedic procedures to repair rotator cuff tears, Bankart lesions, and other joint injuries.
Suture anchors are inserted into pre-drilled holes in the bone and provide a secure fixation point for the sutures, allowing the soft tissue to heal back to the bone.
These devices come in a variety of materials, sizes, and designs to accommodate different anatomical locations and surgical needs.
Proper selection and placement of suture anchors are critical for successful outcomes in suture anchor-based procedures.
Researchers can leverage PubCompare.ai to optimizie sutre anchor protocols through AI-driven comparisons of published literature, pre-prints, and patents, enhancing reproducibility and accuracy in their suture anchor studies.

Most cited protocols related to «Suture Anchors»

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Publication 2010
Amputation Stumps Anesthesia Animals Buprenorphine Collagen Cortex, Cerebral delrin Drill Elbow Femur Fentanyl Intramuscular Injection Joints Knee Ligaments Management, Pain Operative Surgical Procedures Physical Examination Pigs Platelet-Rich Plasma Porifera Saline Solution Sterility, Reproductive Suture Anchors Sutures Synovial Fluid Tibia Vicryl
On February 18, 2009, we performed a systematic search with the Google™ and Yahoo!® search engines as these contain the largest set of Web pages [1 , 7 ]. Combinations of search terms were used: arthroscopy, simulator, orthopaedic, models, simulation, and trainer. A complementary search was performed in classification code G09B23/28 of the patent database Esp@cenet®. Eight different physical and virtual reality arthroscopy simulators were commercially available. Companies were sent an invitation with the request to provide the simulator for 2 weeks at our institute. Two companies agreed to participate: Toltech Knee Arthroscopy Simulator (Touch of Life Technologies, Aurora, CO, USA) and InsightArthroVR® Arthroscopy Simulator (GMV, Madrid, Spain). The other companies [6 , 9 (link), 19 , 21 , 25 , 29 , 30 ] refrained for various reasons unrelated to financial issues.
The Toltech Knee Arthroscopy Simulator (Simulator A) is a virtual reality simulator for arthroscopic knee surgery with two handles that give haptic feedback (Fig. 1) (Appendix 1). The InsightArthroVR® Arthroscopy Simulator (Simulator B) is a virtual reality simulator for arthroscopic knee and shoulder surgery with a multitool that gives haptic feedback (Fig. 2) (Appendix 1).

A photograph shows a participant performing tasks on Simulator A.

A photograph shows a participant performing tasks on Simulator B.

We recruited 37 participants, including (1) all staff members practicing arthroscopy routinely and present at the time of testing (except the main researcher GMMJK), (2) all residents present at the time of testing, and (3) medical students and researchers of our orthopaedic department. The participants were divided into three groups having different levels of arthroscopic experience: novices who had never performed an arthroscopic procedure, intermediates who had performed up to 59 arthroscopies, and experts who had performed more than 60 arthroscopies. This boundary level of 60 arthroscopies was based on the average opinion of fellowship directors who were asked to estimate the number of operations that should be performed to allow a trainee to perform unsupervised meniscectomies [24 (link)]. Simulator A was evaluated by 22 participants in April 2009 and Simulator B by 22 participants in October 2009 (Fig. 3). One participant had reached a higher level of experience between those times. The corresponding subgroups had similar characteristics (Fig. 3).

A flowchart shows the participant population. Subgroups were made on arthroscopic experience at three levels based on the number of arthroscopies performed: novices (0), intermediates (1–59), and experts (> 60). Seven participants evaluated both simulators. The age in years and the number of attended arthroscopies (“Observation”) are expressed as median with range in parentheses. The number of participants who previously had used a simulator (“Simulator”) or had experience in playing computer games (“Games”) is shown.

All participants were scheduled a maximum period of 30 minutes. They had no opportunity to familiarize themselves with either simulator before the experiment. The researcher showed the selection of exercises and performance of the calibration protocol and tasks for the test.
The assessment of construct validity (time to perform a task) was based on one basic navigation task. As the simulators were unlikely to offer a navigation task that was the same, one navigation task was prescribed that can and could be performed on all simulators for comparison. With the arthroscope placed in the anterolateral portal and the probe in the anteromedial portal, nine anatomic landmarks had to be probed sequentially: medial femoral condyle, medial tibial plateau, posterior horn of the medial meniscus, midsection of the medial meniscus, ACL, lateral femoral condyle, lateral tibial plateau, posterior horn of the lateral meniscus, and midsection of the lateral meniscus [32 (link)]. The participants were asked to repeat this navigation task up to five times in a limit of 10 minutes. The navigation task time was defined as described previously [32 (link)] and determined with a separate video recording of the simulator monitor in which the virtual intraarticular joint is presented. We recorded the median time per experience group for each of five repetitions of the navigation task.
Face validity (realism), educational value, and user-friendliness were determined by giving the participants a second task in which exercise(s) had to be performed that were characteristic for that particular simulator and by asking them to fill out a questionnaire afterward. The exercises were selected by the faculty surgeon (GMMJK) and the company to be sure that they best represented the capability of the simulator. Assistance in performing these exercise(s) was given only if a participant failed to continue for a period of 2 minutes. Task performance was pointed out to the participants. The characteristic exercise chosen for Simulator A was “inspection of the suprapatellar pouch with only the 30° arthroscope.” This exercise is set up in three stages: watching an instruction video of the exercise, performing the exercise once guided by example hint-images in a stepwise sequence, and performing the complete exercise once again without guidance. The exercise chosen for Simulator B was threefold: microfracture technique to treat a cartilage lesion in the femoral condyle, visual exploration and probing of a superior labrum anterior superior lesion, and placement of three suture anchors repairing a Bankart lesion (shoulder instability). All three exercises were preceded by textual instructions and had to be performed once. The questionnaire consisted of questions regarding general information (Fig. 3); face validity of the outer appearance of the simulator, the intraarticular virtual joint, and the virtual instruments (Table 1); educational value; and user-friendliness (Table 2). Questions were answered using a 10-point numerical rating scale (NRS) (eg, 0 = completely unrealistic and 10 = completely realistic) or dichotomous requiring a yes/no answer. A 10-point NRS was chosen as all participants were Dutch and this grading system is used at all educational institutions. A value of 7 or greater was considered sufficient. Thus, we expected the grading to be performed based on uniform interpretation of the NRS. Some questions featured a “not applicable (N/A)” answer option, which could be used solely by novices, as these questions required prior knowledge of the real-life arthroscopic situation. For the same reason, only the answers from the expert and intermediate groups were used on simulator realism and educational value. Only answers from the novice and intermediate groups were used on user-friendliness.

Questions addressing face validity

Face validity aspectQuestion
Outer appearanceWhat is your opinion of the outer appearance of this simulator?
Is it clear in which joint you will be operating?
Is it clear which portals are being used?
Intraarticular jointHow realistic is the intraarticular anatomy?
How realistic is the texture of the structures?
How realistic is the color of the structures?
How realistic is the size of the structures?
How realistic is the size of the intraarticular joint space?
How realistic is the arthroscopic image?
InstrumentsHow realistic do the instruments look?
How realistic is the motion of your instruments?
How realistic does the tissue feel when you are probing?

All questions were answered on a 10-point numerical rating scale.

Questions addressing educational value and user-friendliness

ParameterQuestion
Educational value IThe simulator allows training of joint inspection*
The simulator allows training of therapeutic intervention*
The simulator allows training of joint irrigation*
The variation of exercises offered by the simulator is adequate*
Difference in required skill level between exercises is adequate*
Educational value IIThe simulator is a good way to prepare for a real-life arthroscopic operation*
User-friendliness IHow clear are the instructions to start an exercise on the simulator?
How clear is the presentation of your performance by the simulator?
Is it clear how you can improve your performance?
How motivating is the way the results are presented to improve your performance?
User-friendliness III felt the need to read a manual before operating the simulator*

* Questions requiring a dichotomous yes/no answer; all other questions were answered on a 10-point numerical rating scale.

The presence of normal distributions of task times was assessed by Kolmogorov-Smirnov tests. Owing to small sample sizes and skewed distributions, the task times were analyzed nonparametrically. Construct validity was determined for each simulator independently by using Kruskal-Wallis tests to calculate the overall presence of differences in task times between the three experience groups for each of the five task repetitions. The significance level was adjusted for multiple comparisons with the Bonferroni-Holm procedure (alpha = 0.05) [11 ]; when we detect significant differences we performed pair-wise comparisons between the experience groups separately using Mann-Whitney U tests. The scores of the three separate aspects of face validity of the simulators (Table 1) and User-friendliness I (Table 2) were expressed as mean summary scores of the corresponding questions. Educational Value I (Table 2) was expressed as a sum score of five dichotomous questions and ranged from 0 to 5. The mean summary scores (Face Validity and User-friendliness I) were verified for normality by Kolmogorov-Smirnov tests, expressed as mean and SD, and assessed for differences between both simulators with Student’s t tests. The ordinal scale of Educational Value I was presented as medians with ranges and analyzed using a Mann-Whitney U test. The dichotomous questions (Educational Value II and User-friendliness II) expressed as categorical yes/no answers were presented as frequencies and percentages (%) and analyzed by chi square tests or Fisher’s exact test (in case one or more cells had expected counts less than five). The significance level was adjusted for multiple comparisons with the Bonferroni-Holm procedure (alpha = 0.05) [11 ].
Publication 2011
Anatomic Landmarks Arthroscopes Arthroscopic Surgical Procedures Arthroscopy Bankart Lesions Cartilage Cells Condyle Faculty Feelings Fellowships Femur Horns Joints Knee Joint Meniscectomy Menisci, Lateral Meniscus, Medial Microfractures Operative Surgical Procedures Physical Examination Shoulder Student Students, Medical Surgeons Suture Anchors Task Performance Therapeutics Tibia Tissues Touch Perception
Institutional Animal Care and Use Committee approvals were obtained before initiating this study. Eighteen skeletally immature Yorkshire pigs (30 kg, female, 4 months old) underwent ACL transection and suture repair, as noted in Table 1. Same-gendered animals were chosen to eliminate any interanimal variability due to gender. Immature animals were selected because patients with open physes stand to have the longest period of disability after an ACL tear; thus, studying new treatments in this population is of interest. The animals were randomly assigned to 2 treatment groups. In one group, the ACLs had a complete transection in the midsubstance and a primary suture repair of the tibial stump to the femoral insertion site. Two No. 1 vicryl sutures were secured in the distal ACL, using a variable-depth technique, and an absorbable suture anchor was placed at the back of the femoral notch (TwinFix AB 5.0 Suture Anchor with DuraBraid Suture, Smith and Nephew, Inc, Andover, Massachusetts). DuraBraid sutures were then individually tied to the Vicryl sutures in the distal ACL (Figure 1A), with the knees in resting flexion. The second group had the identical procedure; however, a CPC was added to the wound site before closure of the knee (Figure 1B).
Details of the surgical procedure have been described.29 (link) Postoperatively, animals were allowed unrestrained activity. After recovery from anesthesia, they were permitted to resume normal cage activity and nutrition ad libitum. The animals were weightbearing on the nonoperated leg by 2 hours after surgery, and they regained normal gait within 1 week. At the designated time points, the animals were euthanized. The knees were harvested, and mechanical testing was performed to measure the structural properties of the bone-ACL-bone complex.30 (link),41 (link) After mechanical testing, the knees were processed for histologic examination. In addition, 4 intact knees were identified to serve as intact ACL controls.
Publication 2009
Amputation Stumps Anesthesia Animals Anterior Cruciate Ligament Tear Bone and Bones Disabled Persons Epiphyseal Cartilage Femur Gender Institutional Animal Care and Use Committees Knee Operative Surgical Procedures Patients Sus scrofa Suture Anchors Sutures Tibia Vicryl Woman Wounds
The institutional review board assessed and sanctioned this study. Twelve fresh-frozen human cadaveric shoulder specimens (mean age of 60.7+ 2.1 years) kept at -20 °C, without gross evidence of rotator cuff injury or GT bone cyst, were used for this study. Samples were slowly defrosted to 25 °C for ~ 24 h before dissection and testing. Bone mineral density was measured on the greater tuberosity using dual energy X-ray absorptiometry (DXA) to assess bone quality at the site of the fracture interface prior to testing. Aside from the supraspinatus tendon, all soft tissues were resected from the scapula and humerus, with only the whole humerus and supraspinatus tendon retained. A length of over 3 cm of the supraspinatus tendon was preserved at the bony insertion. After cutting the distal humeral condyle, a humeral shaft length of 20 cm remained. Specimens were kept moist during all phases of dissection, preparation, and testing using normal saline solution. Standardized osteotomies oriented 50o with respect to the humeral shaft were performed at the base of the GT using a thin-blade reciprocating saw. The osteotomy was initiated 2 mm medial to the footprint of the supraspinatus tendon and directly posterior to the bicipital groove. Specimens were randomly apportioned to either the suture bridge repair group (SB group) (n = 6) or double-row suture anchor repair group (DR group) (n = 6). A single orthopedic surgeon completed all fixation constructs for all samples.
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Publication 2019
Bone Cysts Bone Density Bones Condyle Dissection Ethics Committees, Research Fracture, Bone Homo sapiens Humerus Normal Saline Orthopedic Surgeons Osteotomy Rotator Cuff Injuries Scapula Shoulder, Frozen Supraspinatus Suture Anchors Sutures Tendons Tissues
All amputation procedures were performed with the patient in the supine position, under general anesthesia, sterile conditions, and tourniquet control. Preoperative intravenous antibiotics were administered in all cases. Preoperative measurements of lower limb circumference were made 6 cm and 12 cm distal to the tibial plateau. A standard stair-step incision was made approximately 12 cm distal to the tibial plateau, preserving a posterior fasciocutaneous flap extending to the distal Achilles. Dissection was carried down to the underlying muscle fascia. Each of the leg compartments was explored to identify the tibialis anterior (TA), lateral gastrocnemius, peroneus longus, and tibialis posterior muscles. These muscles were marked at resting tension with the ankle and subtalar joints in their neutral positions using sutures set at 1 cm intervals. All muscles of the anterior, lateral, and posterior (both superficial and deep) compartments were disinserted. The distal ends of the tibial, superficial peroneal, deep peroneal, and sural nerves were identified, isolated, and transected. Dissection was carried down to the level of the periosteum of the tibia and fibula, and osteotomies were made at approximately 12 cm and 10 cm, respectively. The anterior tibial, posterior tibial, and peroneal vessels were ligated. The medial and lateral tarsal tunnels were procured from the distal amputated limb via sharp dissection, including 4–5 cm segments of each tunnel’s native tendon contents, and were affixed to the flat of the residual tibia using multiple unicortical suture anchors. AMIs were constructed via coaptation of the TA and lateral gastrocnemius muscles to either end of the tendon portion passing through the proximally positioned tarsal tunnel, and coaptation of the tibialis posterior and peroneus longus muscles to the distally positioned tarsal tunnel. Radiopaque 1–2 mm tantalum beads were embedded in the center of each tarsal tunnel, and in all 4 AMI muscles. In patients 2 and 3, the distal ends of the tibial, superficial peroneal, deep peroneal, and sural nerves were capped with free muscle grafts harvested from the distal amputated limb to establish neuroma-preventing RPNIs. The soft-tissue envelope was then closed in a layered fashion over a single closed suction drain. Finally, a layered compression dressing and standard knee immobilizer was applied (Figs. 24).
Publication 2018
Amputation Ankle Antibiotics, Antitubercular Blood Vessel Dissection Fascia Fibula Figs General Anesthesia Grafts Knee Lower Extremity Muscle, Back Muscle, Gastrocnemius Muscle Tissue Neuroma Osteotomy Patients Periosteum Radio-Opaque acrylic resin Sterility, Reproductive Subtalar Joint Suction Drainage Sural Nerve Surgical Flaps Suture Anchors Sutures Tantalum Tendon, Achilles Tendons Tibia Tibial Muscle, Anterior Tissues Tourniquets

Most recents protocols related to «Suture Anchors»

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Publication 2023
Bone and Bones Bone Marrow Cardiac Arrest Cartilage Cicatrix Cortex, Cerebral General Anesthesia Laceration Ligaments, Coracoacromial Operative Surgical Procedures Patients Perfusion Plant Tubers Pressure Suture Anchors Sutures Tendons Tissues
The three-dimensional finite element knee model including the patella, the tendon of the patella, and the distal femur was reconstructed from the CT data of the right knee of a 50-year-old female subject. The IPFP model was created by transecting the patella model at the distal pole of the patella. Then, standard surgical techniques were simulated to instrument the ATBW, SVW, and SVW-BSAG fixation constructs into the IPFP models, which were built to simulate and compare the biomechanical characteristics of the three fixation types.
Two cannulated screws (3 mm in diameter) and a cable (2 mm in diameter) were applied to form the ATBW model, which is a modified tension band fixation (Additional file 1: Figure S1A). The SVW model is built with a cannulated screw (3 mm in diameter) and a cable (2 mm in diameter). In this model, the IPFP injury was only fixed by separate vertical wiring (Additional file 1: Figure S1B). The SVW-BSAG model is built with a cannulated screw (3 mm in diameter), a cable (2 mm in diameter), and two suture anchors (2 mm in diameter). In this model, the cannulated screw and the cable were implanted as in the SVW model. The suture anchor was angled 45 degrees below the horizontal with implantation into the proximal patellar fragment, and the anchor lines were simplified into an irregular cylinder with a diameter of 1 mm fixed on bilateral anchors and the patellar tendon (Additional file 1: Figure S1C). The elements and nodes of the three models are shown in Additional file 1: Table S1.
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Publication 2023
Femur Injuries Knee Ligamentum Patellae Operative Surgical Procedures Ovum Implantation Patella Suture Anchors Woman
Patients were placed supine on the operating table. After anesthesia, routine disinfection and preparation of towels were performed. The midline skin incision approach of the patella was used in all patients to expose the whole patella. After eliminating the clots and periosteum in the fracture gap, reduction in fragments was performed under direct vision.
In the ATBW group, two guide pins were inserted in parallel into the patella and perpendicularly across the fracture. The position of the guide pin was adjusted according to the anteroposterior and lateral C-arm radiographs until the position of the pin was satisfactory. Cannulated screws were inserted along with the guide pin, and then a cable or wire was fixed as a figure-of-8 tension band through the cannulated screws.
In the SVW-BSAG group, a single guide pin was inserted into the patella along the long axis of the patella and perpendicularly across the fracture. The position of the guide pin was adjusted according to the anteroposterior and lateral C-arm radiographs until the position of the pin was satisfactory. After a cannulated screw was inserted along the guide pin, a cable was separated by vertical wiring through the cannulated screw (Fig. 1A–B).

The operation diagram of SVW-BSAG fixation in the IPFP. A AP view and lateral view of the IPFP. B The IPFP reduction was performed, and an SVW technique through cannulated screws and cables was used to fix the fracture. C Two suture anchors were imbedded in the proximal fragment on both sides of the patella. D Separate vertical wiring plus bilateral anchor girdle suturing fixation

Two suture anchors were placed into both sides of the proximal fragment (Fig. 1C). The entry portal of the anchor was at least 1 cm proximal to the transverse fracture line on the coronal plane and approximately 5 mm posterior to the anterior cortical surface on the cross section. Then, the anchor suture string was sutured along the inferior border of distal fragments on the patellar tendons and knotted with one of the contralateral anchor lines at the entry portal of the contralateral anchor (Fig. 1D). The same procedure was repeated for the remaining three anchor lines (Fig. 1D).
In the two groups, patients were required to wear a hinged knee brace for 2 weeks postoperatively. For the first 2 weeks postoperatively, the hinged knee brace was locked in full extension during weight bearing and unlocked when patients were to perform flexion and extension of the knee without weight bearing. Weight-bearing knee flexion and extension exercises were allowed 2 weeks after the operation. Normal passive full-range motion of the knee was required at 4 weeks postoperatively.
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Publication 2023
Anesthesia Braces Clotrimazole Cortex, Cerebral Disinfection Epistropheus Fracture, Bone Knee Ligamentum Patellae Operating Tables Passive Range of Motion Patella Patients Periosteum Skin Suture Anchors Vision X-Rays, Diagnostic
The femur was identified as a rigid body. The other models and implants were identified as linear elastic isotropic materials. The elastic moduli of the patella, patellar tendon, cannulated screw, suture anchor and anchor line were set as 15 GPa, 660 MPa, 110 GPa, 110 GPa, and 200 MPa, respectively, according to material properties and practices [12 (link)–14 (link)]. The Poisson's ratio of the patella, cannulated screw, and suture anchor was 0.3. The Poisson's ratios of the patellar tendon and anchor line were 0.4 and 0.36, respectively (Table 1). The friction coefficient at the anchor-bone interface was 0.6. Starting with a preload of 30 N, the anchoring system was strained.

The Properties of the materials in the biomechanical test

PatellaCartilagePatellar tendonCannulated screwCableSuture AnchorAnchor lineFemur
SpecificationThickness:3 mmdiameter:3.0 mmDiameter: 2 mmdiameter: 1 mmdiameter:0.5 mm
Elastic modulus15GPa5 MPa660 Mpa110GPa110GPa110GPa200 MPaRigid
Poisson's radio0.30.460.40.30.30.30.36
The change in the fracture gap and stress distribution on the components of the models were employed to evaluate the stability of different fixation types. Three paired points were defined on the proximal fragment and distal fragment of the patella to evaluate the displacement of fragments after loading. All of the finite element analyses were completed in ANSYS 17.0.
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Publication 2023
Bone Anchors Femur Fracture, Bone Friction Human Body Ligamentum Patellae Muscle Rigidity Patella Suture Anchors
All patients underwent the shoulder arthroscopic surgery with the same surgical technique and all surgeries were performed by the same surgeons. After receiving general anesthesia combined with interscalene plexus block, all patients were placed in the lateral decubitus position. Normal saline containing epinephrine (1 mg/3 L) was used for intra-articular irrigation. A standardized arthroscopic approach for surgery was used with all patients.
First, an arthroscopic intra-articular examination was performed in all cases to probe whether the patients had other intra-articular lesions. We used 1 to 2 suture anchors (4.5 mm, TWINFIX Ultra PK Suture Anchor, Smith & Nephew) to repair the subscapularis if the subscapularis tendon was torn and recored the type of subscapularis tendon tears. Meanwhile, we performed a biceps tenotomy if the patients had a superior labrum anterior and posterior (SLAP) lesion or degenerative biceps tendon.
Then, via subacromial space arthroscopic vision, we performed acromiolpasty in cases with subacromial impingement syndorme and recored the type of postero-superior cuff tears. The double-row suture-bridge technique was used to repair the cuff tears (4.5 mm, Healix Healix Anchor System, Depuy and 4.5 mm, TWINFIX Ultra PK Suture Anchor, Smith & Nephew). Irreparable type C4 postero-superior cuff tears were eliminated from this study.
At the end of the operation, using a 14G puncture needle, 10 ml of TXA (100 mg/ml) or normal saline was injected into the shoulder joint through a posterior approach.
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Publication 2023
Arthroscopes Arthroscopic Surgical Procedures Epinephrine General Anesthesia Joints Laceration Needles Normal Saline Patients Punctures Shoulder Shoulder Impingement Syndrome Shoulder Joint Subscapularis Surgeons Suture Anchors Suture Techniques Tears Tendons Tenotomy Vision

Top products related to «Suture Anchors»

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FiberWire is a high-strength, non-absorbable suture material used in medical procedures. It is composed of a braided polyethylene fiber construction.
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The PushLock is a surgical implant device designed for use in orthopedic procedures. It is a bioabsorbable tack used to secure soft tissue to bone. The core function of the PushLock is to provide fixation and attachment of soft tissue structures during the healing process.
Fastin RC 3.5 mm is a surgical instrument used in orthopedic procedures. It is a reamer device designed for the preparation of bone cavities.
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The Osteoraptor is a high-precision lab equipment designed for conducting advanced orthopedic research. It features a specialized mechanical system that can accurately simulate and measure various biomechanical properties of bone and joint structures.
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The FiberTak is a laboratory equipment product designed for medical and scientific applications. It is used for securing and positioning various types of materials, such as tissues or samples, during laboratory procedures. The FiberTak provides a secure and adjustable attachment point, allowing researchers and technicians to precisely control the positioning and orientation of the materials being studied.
The Biocorkscrew is a surgical instrument designed for use in orthopedic procedures. It is a corkscrew-like device used to attach soft tissue to bone during reconstruction or repair.
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Twinfix is a surgical implant used in orthopedic procedures. It is a device designed to secure soft tissue to bone. The core function of Twinfix is to provide a means for fixation and stabilization during surgical interventions.
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SPSS is a software package used for statistical analysis. It provides a graphical user interface and a robust set of tools for data manipulation, analysis, and visualization. SPSS is designed to handle a wide range of data types and supports a variety of statistical techniques, including regression analysis, factor analysis, and time series analysis.
The 5.0-mm polyetheretherketone anchor is a medical device designed for use in orthopedic procedures. It is made of a durable, biocompatible polymer material. The anchor is used to secure soft tissue to bone during surgical repairs.
The Swivelock C is a piece of lab equipment designed to securely hold and manipulate samples or specimens. It features a rotational mechanism that allows for precise positioning and adjustment of the held object.

More about "Suture Anchors"

Suture anchors, also known as soft tissue fixation devices, are small implants used in orthopedic procedures to attach tendons, ligaments, or other soft tissues to bone.
These versatile tools are commonly employed in the repair of rotator cuff tears, Bankart lesions, and other joint injuries.
Suture anchors come in a variety of materials, sizes, and designs, such as FiberWire, PushLock, Fastin RC 3.5 mm, Osteoraptor, FiberTak, Biocorkscrew, and Twinfix, to accommodate different anatomical locations and surgical needs.
Proper selection and placement of these anchors are crucial for successful outcomes in suture anchor-based procedures.
Researchers can leverage PubCompare.ai, a powerful AI-driven tool, to optimize suture anchor protocols by comparing published literature, pre-prints, and patents, enhancing the reproducibility and accuracy of their studies.
By identifying best practices and the most effective products, scientists can ensure their suture anchor research is as robust and reliable as possible.
Whether you're working with a 5.0-mm polyetheretherketone anchor or the Swivelock C, PubCompare.ai can help you navigate the landscape of suture anchor technologies and techniques, mitigating the risk of typos or other errors along the way.