ClearanceBrief
510(k) K061082 ยท MQP Spinal Vertebral Body Replacement Device

MOBIS SPINAL IMPLANT

ApplicantSignus Medizintechnik GmbH, Minneapolis MN, US
DecisionSubstantially Equivalent, Dec 18, 2006
ReceivedApr 18, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K061082

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.