510(k) K934429 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANTERIOR SPINE SYSTEM
| Applicant | Buckman Co., Inc., Concord CA, US |
| Decision | Substantially Equivalent, Oct 20, 1994 |
| Received | Sep 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934429
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.