510(k) K090767 ยท MRW System, Facet Screw Spinal Device
PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
| Applicant | Interventional Spine, Inc., Irvine CA, US |
| Decision | Unknown, Jun 11, 2009 |
| Received | Mar 23, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090767
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.