510(k) K930657 ยท KWP Appliance, Fixation, Spinal Interlaminal
D-C-S SYSTEM
| Applicant | Pina-Vertriebs, Switzerland, CH |
| Decision | Unknown, Jun 29, 1994 |
| Received | Feb 9, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930657
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.