510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K173526Substantially Equivalent

SENTIO MMG Gen 2

Medos International SARL, Lelocle, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K173526 is the FDA 510(k) clearance record for SENTIO MMG Gen 2, a class II device, cleared for Medos International SARL on under FDA product code PDQ (Neurosurgical Nerve Locator). FDA's definition for product code PDQ reads: "To locate or monitor function of spinal nerve roots or peripheral nerves during neurosurgery". FDA records list 101 510(k) clearances for Medos International SARL, from to . As of , FDA records show no recalls naming K173526.

Clearance record

Decision date
Received
(142 days to decision)
Product code
PDQ Neurosurgical Nerve Locator
Regulation
21 CFR 874.1820
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Medos International SARL Chemin-Blanc 38, Lelocle, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PDQ

Trailing 12 months
2 clearances under product code PDQ in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PDQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260