ClearanceBrief
510(k) K863147 ยท HTW Bit, Drill

GLENOID DRILL

ApplicantBowen & Company, Inc., Rockville MD, US
DecisionSubstantially Equivalent, Sep 5, 1986
ReceivedAug 15, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863147

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.