The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Arthrex Fibertak Anchors.
| Device ID | K151230 |
| 510k Number | K151230 |
| Device Name: | Arthrex FiberTak Anchors |
| Classification | Fastener, Fixation, Nondegradable, Soft Tissue |
| Applicant | Arthrex, Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Contact | Ivette Galmez |
| Correspondent | Ivette Galmez Arthrex, Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Product Code | MBI |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-08 |
| Decision Date | 2015-06-19 |
| Summary: | summary |