ClearanceBrief
510(k) K091406 ยท MQP Spinal Vertebral Body Replacement Device

ATLAS SPINE SPACER

ApplicantAtlas Spine, LLC, Jupiter FL, US
DecisionSubstantially Equivalent, Sep 4, 2009
ReceivedMay 12, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091406

DateFirm and productCodeLinked 510(k)
Jul 26, 2013Atlas Spine, Inc.
Atlas Spine Torque Limiting Handle 6N-m, P/N 70089 Model # ITN-001-000 Used to rotate implant into position
Terminated
MQPNone listed

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