ClearanceBrief
510(k) K050850 ยท MQP Spinal Vertebral Body Replacement Device

XPAND CORPECTOMY SPACER

ApplicantGlobus Medical, Inc., Phoenixville PA, US
DecisionSubstantially Equivalent, May 26, 2005
ReceivedApr 4, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K050850

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.