ClearanceBrief
510(k) K962628 ยท KWP Appliance, Fixation, Spinal Interlaminal

MOSS MIAMI SPINAL SYSTEM

ApplicantDepuy, Inc., Warsaw IN, US
DecisionSubstantially Equivalent for Some Indications, Mar 18, 1997
ReceivedJul 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962628

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.