510(k) K950209 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
J.B.S. ANTERIOR SPINE SYSTEM(R)
| Applicant | J.B.S. (Usa), Inc., Foster City CA, US |
| Decision | Substantially Equivalent for Some Indications, Oct 11, 1995 |
| Received | Jan 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950209
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.