The following data is part of a premarket notification filed by Arthrex Inc. with the FDA for Arthrex Corkscrew Ft.
| Device ID | K173788 |
| 510k Number | K173788 |
| Device Name: | Arthrex Corkscrew FT |
| Classification | Fastener, Fixation, Biodegradable, Soft Tissue |
| Applicant | Arthrex Inc. 1370 Creekside Boulevard Napes, FL 34108 -1945 |
| Contact | David L Rogers |
| Correspondent | David L Rogers Arthrex Inc. 1370 Creekside Boulevard Naples, FL 34108 -1945 |
| Product Code | MAI |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-14 |
| Decision Date | 2018-03-01 |
| Summary: | summary |