510(k) K990032 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
MODULAR PROTUSIO CUP
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 18, 1999 |
| Received | Jan 6, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990032
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 17, 2020 | Biomet, Inc. RINGLOC ACETABULAR SYSTEM Self-tapping bone screws, Item numbers 103531, 103533, 103534, 103535 - Product Usage: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented; Prosthesis, Hip, Semi-Const Terminated |
LPH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.