ClearanceBrief
510(k) K032094 ยท KWP Appliance, Fixation, Spinal Interlaminal

PASSMED SPINAL SYSTEM

ApplicantMedicrea, Round Rock TX, US
DecisionSubstantially Equivalent, Nov 14, 2003
ReceivedJul 7, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032094

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.