510(k) K993583 ยท ETA Replacement, Ossicular Prosthesis, Total
ZURICH TITANIUM OSSICULAR REPLACEMENT SYSTEM
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Nov 10, 1999 |
| Received | Oct 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993583
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.