ClearanceBrief
510(k) K962824 ยท FZE Prosthesis, Nose, Internal

IMPLANTECH JEJ PERI-PYRIFORM IMPLANT

ApplicantImplantech Associates, Inc., Washington DC, US
DecisionSubstantially Equivalent, Oct 3, 1996
ReceivedJul 19, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962824

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.