510(k) K021507 ยท KWP Appliance, Fixation, Spinal Interlaminal
PLUS PIVOT LINK UNIVERSAL SYSTEM
| Applicant | Spine Vision, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Aug 1, 2002 |
| Received | May 9, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021507
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.