Alamo C

FDA UDI

Class II (US FDA UDI)

by Alliance Partners Llc

Identity

Trade Name: Alamo C FDA UDI
Generic Name: Polymeric spinal interbody fusion cage FDA UDI
Device Name: Cervical Interbody Fusion Device, Titanium FDA UDI
Model / Reference: 0100-1406 FDA UDI
Description: Cervical Interbody Fusion Device, Titanium FDA UDI

Identifiers

Catalog Number: 0100-1406 FDA UDI
Primary DI / UDI-DI: M686010014060 FDA UDI
510(k) Number: K173128 FDA UDI
FDA Product Code: ODP FDA UDI
GMDN Term: Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3080 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Width — 14 Millimeter FDA UDI
Height — 6 Millimeter FDA UDI
Length — 12 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Alamo C by Alliance Partners Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

L-Box® — Innovasis, Inc. · Class II
CoRoent — Nuvasive, Inc. · Class II
Novel Spinal Spacer System — ALPHATEC SPINE, INC. · Class II
S-LIFT® — SPINEFRONTIER, INC. · Class II
Peridot Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
TAURUS PEEK Cage System — Medyssey Co., Ltd. · Class II
Cross-Fuse® II PEEK IBF System — Rti Surgical, Inc. · Class II
Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II

Cleared under the same submission

K173128 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Alliance Partners Llc

Sources (1)

FDA UDI a75e4406-4e7d-44ad-a584-44b415eb17ff 37 fields · synced May 30, 2026