ClearanceBrief
510(k) K092070 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

INTERPLATE C

ApplicantRsb Spine, LLC, Chesterland OH, US
DecisionSubstantially Equivalent, Oct 6, 2009
ReceivedJul 8, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092070

No recall in the FDA data names this 510(k).

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