The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Arthrex Retrofusion Screw.
| Device ID | K151078 |
| 510k Number | K151078 |
| Device Name: | Arthrex RetroFusion Screw |
| Classification | Screw, Fixation, Bone |
| Applicant | ARTHREX, INC. 1370 CREEKSIDE BOULEVARD Naples, FL 34108 -1945 |
| Contact | David L Rogers |
| Correspondent | David L Rogers ARTHREX, INC. 1370 CREEKSIDE BOULEVARD Naples, FL 34108 -1945 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-04-22 |
| Decision Date | 2015-05-15 |
| Summary: | summary |