510(k) K123232 ยท KWP Appliance, Fixation, Spinal Interlaminal
SPINEOLOGY SPINOUS PROCESS PLATE
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Feb 7, 2013 |
| Received | Oct 16, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123232
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.