ClearanceBrief
510(k) K101252 ยท GAT Suture, Nonabsorbable, Synthetic, Polyethylene

NEOTRACT ANCHOR SYSTEM MODEL: REF 11208

ApplicantNeotract, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, Jul 15, 2010
ReceivedMay 4, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101252

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.