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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K233084

Peridot-PT Anterior Cervical Intervertebral body fusion System, Peridot-PT Intervertebral body fusion system · Gbs Commonwealth Co., Ltd. · decided 2023-11-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Peridot-PT Intervertebral body fusion systemL513-0059GBS Commonwealth Co.,Ltd.MAX08800167318022
Peridot-PT Intervertebral body fusion systemL513-0058GBS Commonwealth Co.,Ltd.MAX08800167318015