510(k) K101112 ยท KWP Appliance, Fixation, Spinal Interlaminal
RELIANCE SPINAL SCREW SYSTEM
| Applicant | Reliance Medical Systems, Bountiful UT, US |
| Decision | Substantially Equivalent, Nov 4, 2010 |
| Received | Apr 21, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101112
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.