ClearanceBrief
510(k) K063489 ยท GXD Generator, Lesion, Radiofrequency

STRYKER INTRADISCAL RF GENERATOR

ApplicantSynergetics, Inc., Valley Forge PA, US
DecisionSubstantially Equivalent, May 23, 2007
ReceivedNov 17, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063489

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.