FDA 510(k), K222210, AEON Endoscopic Stapler

FDA 510(k), K222210, AEON Endoscopic Stapler

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510(K) Number: K222210
Device Name: AEON Endoscopic Stapler
Manufacturer: Rainer Maas
Device Classification Name: Staple, Implantable
Regulation Number: GDW
Classification Product Code: 07/25/2022
Date Received: 04/21/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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