ABTross Alif Expandable Cage System

ABTross Alif Expandable Cage System uses titanium alloy interbody cages that expand in height after insertion in an unexpanded state. Serrated upper and lower endplate surfaces contact the…

Registry build 21.09.26

ABTross Alif Expandable Cage System uses titanium alloy interbody cages that expand in height after insertion in an unexpanded state. Serrated upper and lower endplate surfaces contact the vertebral bone, and different widths, lengths, heights and lordotic angles accommodate anatomy.

The system treats degenerative disc disease at one or two contiguous lumbar levels from L2 to S1 in skeletally mature patients after at least six months of nonoperative treatment. Up to Grade 1 spondylolisthesis or retrolisthesis may be present.

Listed Item

ALIF 24x32x12~16mm, 25°

Graft and Fixation

Cages require autogenous or allogeneic cancellous or corticocancellous bone graft and supplemental lumbosacral fixation. Devices with at least 20 degrees of lordosis require anterior supplemental fixation at minimum. Implants are supplied sterile and are intended for single use.

14manufacturers in China registered for this device type
44catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for ABTross Alif Expandable Cage System
Listed by Aegis Spine, United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
510(k) K221719
Record published 2022-11-14
Record revised 2025-07-14 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for ABTross Alif Expandable Cage System
Catalogue number Size Status
2432-2512S In distribution
2432-1512S In distribution
2938-1209S In distribution
2938-1215S In distribution
2432-3015S In distribution
2938-2009S In distribution
2432-0809S In distribution
2938-2509S In distribution
2432-2015S In distribution
2432-2009S In distribution
2938-0809S In distribution
2938-1515S In distribution
2938-3012S In distribution
2432-2012S In distribution
2938-1509S In distribution
2432-0812S In distribution
2938-1212S In distribution
2432-1509S In distribution
2938-3006S In distribution
2938-2506S In distribution
2938-2515S In distribution
2938-2512S In distribution
2938-3015S In distribution
2432-0815S In distribution
2432-2006S In distribution
2432-2506S In distribution
2938-2012S In distribution
2432-1212S In distribution
2432-1515S In distribution
2938-2006S In distribution
2432-3009S In distribution
2432-3006S In distribution
2432-3012S In distribution
2432-1215S In distribution
2432-2515S In distribution
2432-1209S In distribution
2938-1512S In distribution
2938-0815S In distribution
2938-2015S In distribution
2938-3009S In distribution
2432-1506S In distribution
2938-1506S In distribution
2432-2509S In distribution
2938-0812S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K221719 2022-11-03
K203531 2021-01-29

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

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