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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