ClearanceBrief
510(k) K232822 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical

Peridot-TD Spacer system (The Peridot-TD Intervertebral body fusion system), Anterior cervical interbody fusion - ACIF (The Peridot-TD Anterior Cervical Intervertebral body fusion system)

ApplicantGbs Commonwealth Co., Ltd., Geumcheon-Gu, KR
DecisionSubstantially Equivalent, Oct 13, 2023
ReceivedSep 13, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K232822

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.