510(k) K120597 ยท MRW System, Facet Screw Spinal Device
KOMPREDA
| Applicant | Custom Spine, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, May 3, 2013 |
| Received | Feb 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120597
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.