ClearanceBrief
510(k) K172019 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Brisbane ALIF Device, Gladstone ALIF Device

ApplicantSignature Orthopaedics Pty, Ltd., Lane Cove West, AU
DecisionSubstantially Equivalent, Nov 29, 2017
ReceivedJul 5, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172019

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.