ClearanceBrief
510(k) K130830 ยท NQW Orthosis, Spine, Plate, Laminoplasty, Metal

INTEGRA LAMINOPLASTY SYSTEM

ApplicantSeaspine, Inc., Vista CA, US
DecisionSubstantially Equivalent, May 9, 2013
ReceivedMar 26, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130830

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.