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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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