510(k) K902259 ยท JWX Kit, Screening, Staphylococcus Aureus
AXIOM TOTAL KNEE SYSTEM, TIBIAL COMPONENT
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent for Some Indications, Jun 18, 1990 |
| Received | May 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902259
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.