ClearanceBrief
510(k) K072407 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

BODYFORM THORACIC FIXATION SYSTEM

ApplicantTheken Spine, LLC, Akron OH, US
DecisionSubstantially Equivalent, Dec 21, 2007
ReceivedAug 27, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072407

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.