510(k) K121877 ยท KWP Appliance, Fixation, Spinal Interlaminal
GIBRALT OCCIPITAL PLATE SCREWS, SET SCREW, GIBRALT OCCIPITAL SYSTEM ARTICULATING ROD, GIBRALT OCCIPITAL PLATES
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Feb 12, 2013 |
| Received | Jun 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121877
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.