ClearanceBrief
510(k) K781443 ยท KWP Appliance, Fixation, Spinal Interlaminal

HARRINGTON SPINE INSTRUMENTATION

ApplicantOrthopedic Equipment Co., Inc., Walker MI, US
DecisionSubstantially Equivalent, Sep 27, 1978
ReceivedAug 23, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781443

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.