510(k) K110183 ยท NDN Cement, Bone, Vertebroplasty
ARTHROCARE PARALLAX CONTOUR VERTEBRAL AUGMENTATION DEVICE
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Feb 16, 2011 |
| Received | Jan 21, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110183
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.