510(k) K051623 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
ANATOMICAL SHOULDER KEELED GLENOID
| Applicant | Zimmer GmbH, Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 19, 2005 |
| Received | Jun 20, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051623
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 6, 2012 | Zimmer, Inc. zimmer Anatomical Shoulder Glenoid S, cemented, sterile; REF 01.04214.340
PE Keeled Glenoid S, cemented, sterile; REF 01.04214.345,
Glenoid M, cemented, sterile; REF 01.04214.370,
Glenoid L, cement Terminated |
KWS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.