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FDA 510(k) Applications Submitted by Sungji Yoon
FDA 510(k) Number
Submission Date
Device Name
Applicant
K233839
12/04/2023
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
GBS Commonwealth Co., Ltd.
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