ClearanceBrief
510(k) K150455 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

RT2 Trabeculite Titanium Cervical Cage System

ApplicantRhausler, Inc., San Carlos CA, US
DecisionSubstantially Equivalent, Nov 19, 2015
ReceivedFeb 20, 2015
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K150455

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.