ClearanceBrief
510(k) K982320 ยท KWP Appliance, Fixation, Spinal Interlaminal

DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM

ApplicantDepuy, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Sep 14, 1998
ReceivedJul 2, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982320

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.