510(k) K072969 ยท NQP Posterior Metal/Polymer Spinal System, Fusion
DSS
| Applicant | Paradigm Spine, LLC, Washington DC, US |
| Decision | Unknown, Jan 24, 2008 |
| Received | Oct 22, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072969
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.