ClearanceBrief
510(k) K121620 ยท DZI Drill, Bone, Powered

ULTRASONIC SURGERY

ApplicantDmetec.Co., Ltd., Los Angeles CA, US
DecisionSubstantially Equivalent, Dec 11, 2012
ReceivedJun 1, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121620

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.