510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K250725Substantially Equivalent

Hugo™ RAS System

Medtronic, Inc., North Haven CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K250725 is the FDA 510(k) clearance record for Hugo™ RAS System, a class II device, cleared for Covidien, LLC on under FDA product code SCV (Modular Electromechanical Surgical System). FDA's definition for product code SCV reads: "A modular electromechanical surgical system is a software-controlled electromechanical system with a plurality of individual, fully positionable patient/device interfaces which allows a qualified user to perform surgical techniques during...". FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K250725.

Clearance record

Decision date
Received
(268 days to decision)
Product code
SCV Modular Electromechanical Surgical System
Regulation
21 CFR 878.4964
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Covidien, LLC 60 Middletown Ave., North Haven CT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code SCV

Trailing 12 months
3 clearances under product code SCV in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code SCV, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260