ClearanceBrief
510(k) K150994 ยท PHM Intervertebral Fusion Device With Bone Graft, Thoracic

NuVasive CoRoent Thoracolumbar Implants

ApplicantNu Vasive, Incorporated, San Diego CA, US
DecisionSubstantially Equivalent, Jun 17, 2015
ReceivedApr 15, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K150994

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.