510(k) K050391 ยท KWP Appliance, Fixation, Spinal Interlaminal
PROTEX CT CERVICOTHORACIC SPINAL SYSTEM
| Applicant | Globus Medical, Inc., Phoenixville PA, US |
| Decision | Substantially Equivalent, Jul 21, 2005 |
| Received | Feb 16, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050391
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.