FDA.reportPublic FDA data

510(k) K233839

Device
Peridot-PT Anterior Cervical Intervertebral body fusion System; Peridot-PT Intervertebral body fusion system; The Peridot-TD Anterior Cervical Intervertebral body fusion system; The Peridot-TD Intervertebral body fusion system
Applicant
Gbs Commonwealth Co., Ltd.
510(k) number
K233839
Product code
ODP
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-20
Date received
2023-12-04
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Cervical
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Sungji Yoon
Address
C-309. Woolim Lion'S Valley, 168, Gasan Digital 1-Ro Geumcheon-Gu KR 08507 08507

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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