ClearanceBrief
510(k) K091228 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SPINEWAND SURGICAL DEVICE

ApplicantArthrocare Corp., Sunnyvale CA, US
DecisionSubstantially Equivalent, Sep 28, 2009
ReceivedApr 27, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K091228

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.