ClearanceBrief
510(k) K973924 ยท JEY Plate, Bone

FRIOS BONESHIELD

ApplicantFriatec AG, Potomac MD, US
DecisionSubstantially Equivalent, May 7, 1998
ReceivedOct 15, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973924

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.