ClearanceBrief
510(k) K864337 ยท

SEGMENTAL SPINAL INSTRUMENTATION SYSTEM

ApplicantKirschner Medical Corp., Timonium MD, US
DecisionSubstantially Equivalent, Dec 16, 1986
ReceivedNov 4, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864337

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.