Alamo T 2100T-2806

by Alliance Partners LLC

Alamo T 2100T-2806 is a Class I device made by Alliance Partners LLC, cleared under FDA 510(k) K140303 on 21 Apr 2014 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI M6862100T28060), 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

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberM6862100T28060 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Special	NumberK140303	Date21 Apr 2014Decided	StatusActive

Official records

FDA 510(k) database 510(k) number K140303

Across registries

2 registries list this device

FDA 510(k) K140303 decided 21 Apr 2014 Active
FDA GUDID UDI-DI M6862100T28060 listed 23 Sep 2016 Listed

Timeline

2 dated events

21 Apr 2014 Cleared FDA 510(k) K140303
23 Sep 2016 Listed FDA GUDID M6862100T28060

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Alamo T
Generic name: Spinal implant trial
Model / Ref / Catalog: 2100T-2806

Primary DI / UDI-DI: M6862100T28060
510(k) Number: K140303
FDA product code: HWT
GMDN term: Spinal implant trial

Device class: Class I
Regulation number: 888.4800
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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See all devices from Alliance Partners LLC →

Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)