510(k) K063172 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ARTHROCARE CAVITY SPINEWAND
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Apr 27, 2007 |
| Received | Oct 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063172
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 8, 2016 | ArthroCare Corporation Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in spinal procedures. Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.