510(k) K101083 ยท NQP Posterior Metal/Polymer Spinal System, Fusion
DSS STABILIZATION SYSTEM
| Applicant | Paradigm Spine, LLC, Washington DC, US |
| Decision | Unknown, Jul 2, 2010 |
| Received | Apr 19, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101083
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.