ClearanceBrief
510(k) K050451 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

SYNTHES VECTRA SYSTEM

ApplicantSynthes Spine Co.Lp, West Chester PA, US
DecisionSubstantially Equivalent, Mar 24, 2005
ReceivedFeb 22, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K050451

DateFirm and productCodeLinked 510(k)
Sep 22, 2014Synthes, Inc.
DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level / 34 mm part 04.613.184 3337672 TI Vectra" Plate 3 Level / 57 mm part 04.613.257 lot 3693878 TI Vectra" Plate 4 Level / 64 mm part
Terminated
KWQNone listed
Feb 4, 2013Synthes USA HQ, Inc.
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit, graduated 12mm - 26mm adjustable depth, Part Number 03.613.011. Synthes Vectra System,
Terminated
KWQNone listed
Feb 4, 2013Synthes USA HQ, Inc.
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion, Adjustable Drill Stop, Part Number 03.613.012. Synthes Vectra System, Synthes Vectra-One System and Synth
Terminated
KWQNone listed

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