510(k) K013312 ยท KWP Appliance, Fixation, Spinal Interlaminal
P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
| Applicant | Spine Vision, Inc., Atlanta GA, US |
| Decision | Substantially Equivalent, Feb 13, 2002 |
| Received | Oct 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013312
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.