ClearanceBrief
510(k) K973502 ยท LZK Implant, Malar

IMPLANTECH CONFORM BINDER SUBMALAR IMPLANT

ApplicantImplantech Associates, Inc., Washington DC, US
DecisionSubstantially Equivalent, Nov 7, 1997
ReceivedSep 16, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973502

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.