The following data is part of a premarket notification filed by Arthrex Inc. with the FDA for Univers Revers Modular Glenoid System, Half Augment Baseplate.
| Device ID | K200895 |
| 510k Number | K200895 |
| Device Name: | Univers Revers Modular Glenoid System, Half Augment Baseplate |
| Classification | Shoulder Prosthesis, Reverse Configuration |
| 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 | PHX |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-04-03 |
| Decision Date | 2020-08-13 |