ArthroTAK Tendon Anchor Kit
FDA 510(k) K262809 · ArthroTAK, LLC
510(k) numberK262809
Submission
- Device name
- ArthroTAK Tendon Anchor Kit
- Applicant
- ArthroTAK, LLC
Missoula, MT, US - Received
- August 7, 2026
- Decision date
- September 2, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MBI – Fastener, Fixation, Nondegradable, Soft Tissue
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3040
- Specialty
- Orthopedic
- Implant
- Yes
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| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253065 | Aevumed SUPERCYNCH Button SystemMBI · Traditional | Aevumed, Inc. | 09/02/2026SE |
| K262677 | Iconix Knotless TMBI · Special | Riverpoint Medical | 08/27/2026SE |
| K262047 | Grappler Suture Anchor SystemMBI · Special | Paragon 28, Inc. | 08/03/2026SE |
| K262369 | AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair…MBI · Special | Stryker Endoscopy | 07/30/2026SE |
| K261770 | Suture Button Repair SystemMBI · Traditional | Skeletal Dynamics, Inc. | 07/29/2026SE |
| K261632 | Thunderbolt SystemMBI · Special | Responsive Arthroscopy, Inc. | 07/20/2026SE |
| K261968 | Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE…MBI · Special | Smith & Nephew, Inc. | 07/09/2026SE |
| K260018 | Arthrex FiberButtonMBI · Traditional | Arthrex, Inc. | 06/26/2026SE |
| K253130 | Dione PEEK Screw SystemMBI · Traditional | ZheJiang Decans Medical Devices Co., Ltd. | 05/27/2026SE |
| K261363 | Y-Knotless Flex AnchorsMBI · Special | CONMED Corporation | 05/13/2026SE |
More from CONMED Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K252635 | ArthroTAK Tendon Anchor KitMBI · Traditional | 05/01/2026SE |
Questions and answers
When was ArthroTAK Tendon Anchor Kit cleared by the FDA?
ArthroTAK Tendon Anchor Kit (K262809) received a 510(k) decision of Substantially Equivalent on September 2, 2026, 26 days after the submission was received.
What is the product code of K262809?
The FDA product code is MBI – Fastener, Fixation, Nondegradable, Soft Tissue, a Class II (moderate risk) device regulated under 21 CFR 888.3040.