ClearanceBrief
510(k) K983282 ยท KWP Appliance, Fixation, Spinal Interlaminal

OMI OCCIPITAL CERVICAL LOOP, MODEL A1089

ApplicantOhio Medical Instrument Co., Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Nov 19, 1998
ReceivedSep 18, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983282

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.