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 |