ClearanceBrief
510(k) K121413 ยท GAT Suture, Nonabsorbable, Synthetic, Polyethylene

CROSSFIX II MEMISCAL REPAIR DEVICE

ApplicantCayenne Medical, Inc., Scottsdale AZ, US
DecisionSubstantially Equivalent, Jun 4, 2012
ReceivedMay 11, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K121413

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.