ClearanceBrief
510(k) K092401 ยท LYA Splint, Intranasal Septal

SINEXUS SINUS STENT GEN 2, MODEL 1999-25

ApplicantSinexus, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Nov 17, 2009
ReceivedAug 6, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092401

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.