ClearanceBrief
510(k) K141993 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

NAKOMA ACP

ApplicantAlliance Partners, LLC, Memphis TN, US
DecisionSubstantially Equivalent, Nov 6, 2014
ReceivedJul 22, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K141993

DateFirm and productCodeLinked 510(k)
Jul 7, 2015Alliance Partners LLC
Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for anterior intervertebral screw fixation of the cervical spine at
Terminated
KWQNone listed

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