510(k) K935113 ยท KWP Appliance, Fixation, Spinal Interlaminal
J.B.S. IMPLANTABLE SPINAL FIXATION DEVICE
| Applicant | J.B.S., S.A., Foster City CA, US |
| Decision | Substantially Equivalent, Oct 19, 1994 |
| Received | Oct 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935113
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.