510(k) K902397 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODULOCK POSTERIOR SPINAL FIXATION
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Nov 5, 1990 |
| Received | May 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902397
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.