510(k) K122292 ยท KWP Appliance, Fixation, Spinal Interlaminal
RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM
| Applicant | Reliance Medical Systems, LLC, Bountiful UT, US |
| Decision | Substantially Equivalent, Oct 24, 2012 |
| Received | Jul 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122292
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.