Cleared Traditional

K242157 - Anovo Surgical System (Model 6Ne) (FDA 510(k) Clearance)

Oct 2024
Decision
90d
Days
Class 2
Risk

K242157 is an FDA 510(k) clearance for the Anovo Surgical System (Model 6Ne). This device is classified as a Mountable Electromechanical Surgical System For Transluminal Approaches (Class II - Special Controls, product code QNM).

Submitted by Momentis Surgical , Ltd. (Or Yehuda, IL). The FDA issued a Cleared decision on October 21, 2024, 90 days after receiving the submission on July 23, 2024.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4961. A Mountable Electromechanical Surgical System For Transluminal Approaches Is A Software-controlled, Patient Bed- And/or Operating Table-mounted Electromechanical Surgical System With Human/device Interfaces That Allows A Qualified User To Perform Transluminal Endoscopic Or Laparoscopic Surgical Procedures Using Surgical Instruments Attached To An Electromechanical Arm..

Submission Details

510(k) Number K242157 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 23, 2024
Decision Date October 21, 2024
Days to Decision 90 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code QNM - Mountable Electromechanical Surgical System For Transluminal Approaches
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4961
Definition A Mountable Electromechanical Surgical System For Transluminal Approaches Is A Software-controlled, Patient Bed- And/or Operating Table-mounted Electromechanical Surgical System With Human/device Interfaces That Allows A Qualified User To Perform Transluminal Endoscopic Or Laparoscopic Surgical Procedures Using Surgical Instruments Attached To An Electromechanical Arm.