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EZ-Track CAEB393016M

by Next Orthosurgical

EZ-Track CAEB393016M is a Class II device made by Next Orthosurgical, cleared under FDA 510(k) K131082 on 26 Aug 2013 and listed in FDA GUDID since 12 Sep 2024 (UDI-DI 00840314135506), 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) K131082

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 Number00840314135506 UDI-DI Date12 Sep 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK131082 Date26 Aug 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131082 decided 26 Aug 2013 Active
  • FDA GUDID UDI-DI 00840314135506 listed 12 Sep 2024 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131082
  2. Listed FDA GUDID 00840314135506

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
EZ-Track
Generic name
Polymeric spinal interbody fusion cage
Model / Ref / Catalog
CAEB393016M
Description
ALIF INTERBODY CAGE, 39 X 30 X 16MM -12°
Primary DI / UDI-DI
00840314135506
510(k) Number
FDA product code
MAX
GMDN term
Polymeric spinal interbody fusion cage
Device class
Class II
Regulation number
888.3080
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Width — 39 Millimeter
Length — 30 Millimeter
Height — 16 Millimeter
Angle — 12 degree

Related devices

Category: Polymeric spinal interbody fusion cage

Cleared under the same submission (K131082)

and 8 more cleared under K131082

Similar devices

Other devices filed under FDA product code MAX (Intervertebral Fusion Device With Bone Graft, Lumbar).

Other devices from Next Orthosurgical

See all devices from Next Orthosurgical →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (10, all answered No)