ClearanceBrief
510(k) K113802 ยท NQW Orthosis, Spine, Plate, Laminoplasty, Metal

ESCALATE LAMINOPLASTY SYSTEM

ApplicantStryker Spine, Allendale NJ, US
DecisionSubstantially Equivalent, Apr 16, 2012
ReceivedDec 23, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113802

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.