ClearanceBrief
510(k) K041625 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body

LTD POLYAXIAL FIXATION SYSTEM

ApplicantUs Spinal Technologies, LLC, Stillwater MN, US
DecisionSubstantially Equivalent, Sep 8, 2004
ReceivedJun 15, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041625

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.