ClearanceBrief
510(k) K052413 ยท KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

TUNA SYSTEM, MODELS 8909, 8929, 8930, 8934

ApplicantMedtronic Vascular, Shoreview MN, US
DecisionSubstantially Equivalent, Nov 17, 2005
ReceivedSep 2, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K052413

DateFirm and productCodeLinked 510(k)
Mar 10, 2009Medtronic Neuromodulation
PROSTIVA RF Model 8929 Hand Piece is the delivery system component of the PROSTIVA RF Therapy System. PROSTIVA RF Therapy Kit 8929, Sterilized using ethylene oxide, Manufacturer Medtronic Inc Minneap
Terminated
KNSNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.