ClearanceBrief
510(k) K073505 ยท MQP Spinal Vertebral Body Replacement Device

MODIFICATION TO VALEO VBR

ApplicantAmedica Corp., Washington DC, US
DecisionSubstantially Equivalent, Jan 9, 2008
ReceivedDec 13, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K073505

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.