ClearanceBrief
510(k) K123758 ยท MQP Spinal Vertebral Body Replacement Device

TASMIN R

ApplicantSignus Medizintechnik GmbH, Chesterland OH, US
DecisionSubstantially Equivalent, Jan 14, 2014
ReceivedDec 7, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123758

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.