510(k) K992885 ยท KWP Appliance, Fixation, Spinal Interlaminal
VERSALOK LOW BACK FIXATION SYSTEM
| Applicant | Osteotech, Inc., Eatontown NJ, US |
| Decision | Substantially Equivalent, Nov 19, 1999 |
| Received | Aug 27, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992885
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.