510(k) K230708 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)
| Applicant | Gbs Commonwealth Co., Ltd., Geumcheon-Gu, KR |
| Decision | Substantially Equivalent, May 22, 2023 |
| Received | Mar 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230708
No recall in the FDA data names this 510(k).
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