ClearanceBrief
510(k) K882871 ยท LYQ Accessories, Fixation, Spinal Intervertebral Body

CASF DRILL GUIDE DG 170

ApplicantTerray Manufacturing, Inc., Ontario K7s 1l8, CA
DecisionSubstantially Equivalent for Some Indications, Sep 23, 1988
ReceivedJul 11, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882871

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.