Alamo C 0107-1405

by Alliance Partners LLC

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberM686010714050 UDI-DI	Date18 Apr 2018Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k) from GUDID	NumberK173128	Date22 Mar 2018Issued	StatusActive

Official records

FDA 510(k) database 510(k) number K173128

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Alamo C
Generic name: Polymeric spinal interbody fusion cage
Model / Ref / Catalog: 0107-1405

Primary DI / UDI-DI: M686010714050
510(k) Number: K173128
FDA product code: ODP
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 — 14 Millimeter
Height — 5 Millimeter
Angle — 7 degree
Length — 12 Millimeter

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See all devices from Alliance Partners LLC →

Properties

Sterilise before use
Single use
Implantable
Prescription use
Lot / batch number

Other properties (10)

Supplied sterile: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Premarket exempt: No
Serial number: No
Expiration date: No
Manufacturing date: No