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Cortac 2110-08-124

by Pmt Corp.

Cortac 2110-08-124 is a Class II device made by Pmt Corp., cleared under FDA 510(k) K082474 on 8 May 2009 and listed in FDA GUDID since 29 Jun 2021 (UDI-DI 00650551002062), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K082474

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00650551002062 UDI-DI Date29 Jun 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK082474 Date8 May 2009DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K082474 decided 8 May 2009 Active
  • FDA GUDID UDI-DI 00650551002062 listed 29 Jun 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K082474
  2. Listed FDA GUDID 00650551002062

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Cortac
Generic name
Cortical electrode
Model / reference
2110-08-124
Primary DI / UDI-DI
00650551002062
510(k) Number
FDA product code
GYC
GMDN term
Cortical electrode
Device class
Class II
Regulation number
882.1310
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cortical electrode

Cleared under the same submission (K082474)

and 8 more cleared under K082474

Similar devices

Other devices filed under FDA product code GYC (Electrode, Cortical).

Other devices from Pmt Corp.

See all devices from Pmt Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)