510(k) K032943 ยท KNW Instrument, Biopsy
STRYKER VERTEBRAL BODY AND BONE BIOPSY KITS, STRYKER CAPTURE BODY AND BONE BIOSPSY KITS
| Applicant | Stryker Corp., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Dec 17, 2003 |
| Received | Sep 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032943
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.