ClearanceBrief
510(k) K203444 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

BEE HA Cage

ApplicantNGMedical GmbH, Nonnweiler, DE
DecisionSubstantially Equivalent, Mar 18, 2021
ReceivedNov 23, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203444

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.