ClearanceBrief
510(k) K111449 ยท NKB Thoracolumbosacral Pedicle Screw System

REVOLVE ADDITIONAL IMPLANTS

ApplicantGlobus Medical, Inc., Audubon PA, US
DecisionSubstantially Equivalent, Aug 17, 2011
ReceivedMay 25, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K111449

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.