ClearanceBrief
510(k) K131851 ยท HAE Rongeur, Manual

OSTEOMED NEURO RONGEUR

ApplicantOsteomed, Addison TX, US
DecisionSubstantially Equivalent, Dec 6, 2013
ReceivedJun 21, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131851

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.