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FDA 510(k) Applications Submitted by Kay Kwon
FDA 510(k) Number
Submission Date
Device Name
Applicant
K210035
01/06/2021
ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System
Aegis Spine
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