510(k) K012881 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
C3 ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Spine Vision, Inc., Good Hope GA, US |
| Decision | Substantially Equivalent, Nov 26, 2001 |
| Received | Aug 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012881
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.