ClearanceBrief
510(k) K914715 ยท FZX Guide, Surgical, Instrument

PARALLELING GUIDES

ApplicantImplant Corp. of America, St. Petersburg FL, US
DecisionSubstantially Equivalent, Feb 16, 1994
ReceivedOct 18, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914715

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.