ClearanceBrief
510(k) K063117 ยท GXQ Dura Substitute

MODIFICATION TO DUREPAIR DURA REGENERATION MATRIX

ApplicantMedtronic Neurosurgery, Goleta CA, US
DecisionSubstantially Equivalent, Nov 3, 2006
ReceivedOct 12, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K063117

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.