510(k) K962314 ยท KWP Appliance, Fixation, Spinal Interlaminal
HALIFAX PLUS INTERLAMINAR CLAMP SYSTEM
| Applicant | Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Dec 9, 1996 |
| Received | Jun 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962314
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.