ClearanceBrief
510(k) K041000 ยท GXQ Dura Substitute

DUREPAIR DURA REGENERATION MATRIX

ApplicantMedtronic Neurosurgery, Goleta CA, US
DecisionSubstantially Equivalent, Jul 27, 2004
ReceivedApr 19, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041000

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.