ClearanceBrief
510(k) K060416 ยท MQP Spinal Vertebral Body Replacement Device

OBELISC VERTEBRAL BODY REPLACEMENT DEVICE

ApplicantUlrich GmbH & Co. KG, Clearwater FL, US
DecisionSubstantially Equivalent, Dec 26, 2006
ReceivedFeb 17, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060416

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.