510(k) K954698 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
TRILOGY ACETABULAR COMPONENT 7MM OFFSET
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 17, 1996 |
| Received | Oct 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954698
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 20, 2014 | Zimmer, Inc. TRILOGY ACET SHELL 36MM O
TRILOGY ACET SHELL 38MM O
TRILOGY ACET SHELL 40MM O
TRILOGY ACET SHELL 42MM O
TRILOGY ACET SHELL 44MM O
TRILOGY ACET SHELL 46MM O
TRILOGY ACET SHELL 48MM O
TRILOGY ACET SHELL Terminated |
LPH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.