The following data is part of a premarket notification filed by Zimmer Inc. with the FDA for Alliance Glenoid.
| Device ID | K191814 |
| 510k Number | K191814 |
| Device Name: | Alliance Glenoid |
| Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
| Applicant | Zimmer Inc. P.O. Box 708 Warsaw, IN 46581 -0708 |
| Contact | Patricia Sandborn Beres |
| Correspondent | Patricia Sandborn Beres Zimmer Inc. P.O. Box 708 Warsaw, IN 46581 -0708 |
| Product Code | KWS |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-07-05 |
| Decision Date | 2019-10-23 |
| Summary: | summary |