510(k) K072321 ยท NQP Posterior Metal/Polymer Spinal System, Fusion
BIOFLEX
| Applicant | Biospine Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 25, 2008 |
| Received | Aug 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072321
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.