ClearanceBrief
510(k) K042953 ยท NKB Thoracolumbosacral Pedicle Screw System

MODIFICATION TO PROTEX STABILIZATION SYSTEM

ApplicantGlobus Medical, Inc., Phoenixville PA, US
DecisionSubstantially Equivalent, Nov 22, 2004
ReceivedOct 26, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K042953

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.