510(k) K991678 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
WHITESIDE BIOMECHANICS SPINAL SYSTEM
| Applicant | Whiteside Biomechanics, Inc., Creve Coeur MO, US |
| Decision | Substantially Equivalent, Aug 12, 1999 |
| Received | May 17, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991678
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.