510(k) K072271 ยท HAW Neurological Stereotaxic Instrument
STRYKER NAVIGATION SYSTEM INFINITUS HIP RESURFACING MODULE
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Dec 18, 2007 |
| Received | Aug 15, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072271
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.