510(k) K100479 ยท NDN Cement, Bone, Vertebroplasty
PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Sep 21, 2010 |
| Received | Feb 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100479
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.