ClearanceBrief
510(k) K960807 ยท GZT Retractor, Self-Retaining, For Neurosurgery

TEW CRANIAL/SPINAL RETRACTOR MODEL A1090

ApplicantOhio Medical Instrument Co., Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, May 17, 1996
ReceivedFeb 28, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960807

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.