Skip to content

Quattrode™ 3066

by Advanced Neuromodulation Systems

Quattrode™ 3066 is a Class II device made by Advanced Neuromodulation Systems, cleared under FDA 510(k) K072462 on 11 Oct 2007 (1 earlier submission) and listed in FDA GUDID since 25 Apr 2015 (UDI-DI 05414734401548), active as of 23 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 23 Oct 2026

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05414734401548 UDI-DI Date25 Apr 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK072462 Date11 Oct 2007DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K072462 decided 11 Oct 2007 Active· +1 more in the status table
  • FDA GUDID UDI-DI 05414734401548 listed 25 Apr 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K960728
  2. Cleared FDA 510(k) K072462
  3. Listed FDA GUDID 05414734401548

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Quattrode™
Generic name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
Model / Ref / Catalog
3066
Primary DI / UDI-DI
05414734401548
510(k) Number
FDA product code
GZF, GZB
GMDN term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection
Device class
Class II
Regulation number
882.5870, 882.5880
GUDID distribution status
In Commercial Distribution
Size
Length — 60.0000 Centimeter

Related devices

Category: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wired connection

Cleared under the same submission (K072462)

and 1 more cleared under K072462

Cleared under the same submission (K960728)

and 2 more cleared under K960728

Other devices from Advanced Neuromodulation Systems

  • MN13650

    Class III

  • 1210 Open recall

    Class III

  • Infinity™ 6884 Open recall

    Class III

  • Proclaim™ 3884 Open recall

    Class III

See all devices from Advanced Neuromodulation Systems →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
Other properties (9, all answered No)