ClearanceBrief
510(k) K903151 ยท HAE Rongeur, Manual

INTERVERTEBRAL DISC RONGEUR

ApplicantVon Zeppelin GmbH, Pullach, DE
DecisionSubstantially Equivalent, Dec 11, 1990
ReceivedJul 18, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903151

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.