510(k) K052069 ยท KWP Appliance, Fixation, Spinal Interlaminal
PROTEX STABILIZATION SYSTEM WITH ADDITIONAL COMPONENTES
| Applicant | Globus Medical, Inc., Phoenixville PA, US |
| Decision | Substantially Equivalent, Aug 17, 2005 |
| Received | Aug 1, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052069
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.