ClearanceBrief
510(k) K041911 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

SYNTHES (USA) LCP CURVED PLATES

ApplicantSynthes (Usa), Paoli PA, US
DecisionSubstantially Equivalent, Sep 8, 2004
ReceivedJul 15, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041911

DateFirm and productCodeLinked 510(k)
Nov 27, 2013Synthes USA HQ, Inc.
Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
Terminated
KTTNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.