Alamo C

Alamo C is a cervical interbody fusion cage range with a rectangular profile and a hollow core for autograft bone. The cage occupies the disc space between vertebral endplates as part of an…

Registry build 21.09.26

Alamo C is a cervical interbody fusion cage range with a rectangular profile and a hollow core for autograft bone. The cage occupies the disc space between vertebral endplates as part of an anterior fusion construct.

The range includes PEEK versions with tantalum markers and titanium alloy versions. Ridges on the upper and lower surfaces provide the bone-contact features intended to improve fixation and resist migration.

Listed Item

Cervical Interbody Fusion Device, Titanium

Size and Fixation Options

Different footprints and heights accommodate anatomical variation. The system is used with supplemental fixation and autograft for a single cervical level from C2 through T1; the cage is the interbody component within that larger assembly.

7manufacturers in China registered for this device type
32catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Shandong (2), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ODP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for Alamo C
Listed by Alliance Partners, LLC, United States
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
510(k) K173128
Record published 2018-04-18
Record revised 2020-02-24 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Length 12 to 14 mm; height 5 to 12 mm; width 14 to 17 mm; angle 7 °

Catalogue Numbers

Catalogue numbers for Alamo C
Catalogue number Size Status
0100-1712 Length 14 mm In distribution
0100-1706 Length 14 mm In distribution
0100-1711 Width 17 mm In distribution
0100-1708 Width 17 mm In distribution
0107-1707 Height 7 mm In distribution
0107-1710 Length 14 mm In distribution
0100-1707 Width 17 mm In distribution
0107-1711 Width 17 mm In distribution
0107-1706 Angle 7 ° In distribution
0100-1407 Height 7 mm In distribution
0100-1705 Length 14 mm In distribution
0107-1406 Height 6 mm In distribution
0100-1410 Height 10 mm In distribution
0100-1710 Height 10 mm In distribution
0100-1412 Length 12 mm In distribution
0107-1705 Angle 7 ° In distribution
0100-1709 Width 17 mm In distribution
0100-1405 Width 14 mm In distribution
0107-1407 Width 14 mm In distribution
0107-1412 Length 12 mm In distribution
0107-1709 Width 17 mm In distribution
0107-1411 Length 12 mm In distribution
0100-1409 Width 14 mm In distribution
0100-1411 Height 11 mm In distribution
0107-1708 Angle 7 ° In distribution
0100-1408 Height 8 mm In distribution
0107-1410 Height 10 mm In distribution
0107-1712 Angle 7 ° In distribution
0107-1408 Length 12 mm In distribution
0107-1409 Width 14 mm In distribution
0107-1405 Width 14 mm In distribution
0100-1406 Width 14 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173128 2018-03-22
K133321 2014-01-09
K112361 2011-11-30

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer