ClearanceBrief
510(k) K090841 ยท MQP Spinal Vertebral Body Replacement Device

ADDPLUS

ApplicantUlrich GmbH & Co. KG, St. Louis MO, US
DecisionSubstantially Equivalent, Oct 5, 2009
ReceivedMar 27, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090841

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.