ClearanceBrief
510(k) K933881 ยท KWP Appliance, Fixation, Spinal Interlaminal

DEPUY MOTECH MOSS-MIAMI SPINAL SYSTEM

ApplicantDepuy, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 12, 1994
ReceivedAug 10, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933881

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.