510(k) K082235 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BLACKSTONE PILLAR XL PEEK SPACERS
| Applicant | Blackstone Medical, Inc., Wayne NJ, US |
| Decision | Substantially Equivalent, Sep 4, 2008 |
| Received | Aug 7, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082235
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.