ClearanceBrief
510(k) K213493 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Fortilink with TiPlus Technology

ApplicantParadigm Spine, Wurmlingen Baden-Wurttemberg, DE
DecisionSubstantially Equivalent, Jan 27, 2022
ReceivedNov 1, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213493

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.