510(k) K101704 ยท NQP Posterior Metal/Polymer Spinal System, Fusion
ZIMMER DTO PIN PRESS INSTRUMENT
| Applicant | Zimmer Spine, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 18, 2010 |
| Received | Jun 17, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101704
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.