ClearanceBrief
510(k) K090658 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

SYNTHES EXTERNAL FIXATION DEVICES, MR CONDITIONAL

ApplicantSynthes (Usa), West Chester PA, US
DecisionSubstantially Equivalent, Mar 3, 2010
ReceivedMar 12, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090658

DateFirm and productCodeLinked 510(k)
Jun 19, 2014Synthes, Inc.
Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components.
Terminated
KTTNone listed

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