510(k) DEN190022

Device
Hominis Surgical System
Applicant
Momentis Surgical , Ltd.
510(k) number
DEN190022
Product code
QNM
Decision
Unknown (DENG)
Decision date
2021-02-26
Date received
2019-04-17
Regulation
878.4961
Classification name
Mountable Electromechanical Surgical System For Transluminal Approaches
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Direct
Third party reviewed
N

Applicant Contact#

Contact
Maya Leib Shlomo
Address
6 Yoni Netanyahu St. Or Yehuda IL 6037604 6037604

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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