Alamo P 2100T-2212

by Alliance Partners LLC

Alamo P 2100T-2212 is a Class I device made by Alliance Partners LLC, cleared under FDA 510(k) K122047 on 4 Sep 2012 and listed in FDA GUDID since 30 Sep 2016 (UDI-DI M6862100T22120), 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	NumberM6862100T22120 UDI-DI	Date30 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK122047	Date4 Sep 2012Decided	StatusActive

Official records

FDA 510(k) database 510(k) number K122047

Across registries

2 registries list this device

FDA 510(k) K122047 decided 4 Sep 2012 Active
FDA GUDID UDI-DI M6862100T22120 listed 30 Sep 2016 Listed

Timeline

2 dated events

4 Sep 2012 Cleared FDA 510(k) K122047
30 Sep 2016 Listed FDA GUDID M6862100T22120

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Alamo P
Generic name: Spinal implant trial
Model / Ref / Catalog: 2100T-2212

Primary DI / UDI-DI: M6862100T22120
510(k) Number: K122047
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)