510(k) K093534 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO CASPIAN SPINAL SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Dec 16, 2009 |
| Received | Nov 16, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093534
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.