510(k) K990708 ยท KWP Appliance, Fixation, Spinal Interlaminal
TITANIUM VERSALOK
| Applicant | Wrightmedicaltechnologyinc, Arlington TN, US |
| Decision | Substantially Equivalent, Mar 30, 1999 |
| Received | Mar 4, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990708
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.