Pyxis 3d Titanium Cervical Cage System

171 catalogue numbers from 8062-1608S, listed by GS Medical Co., Ltd., South Korea, under Intervertebral Fusion Device With Bone Graft, Lumbar. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
171catalogue numbers in this listing
4510(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 Pyxis 3D Titanium Cervical Cage System
Listed by GS Medical Co., Ltd., South Korea
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Manufacturer
510(k) K241738
Record published 2025-05-20
Record revised 2026-05-14 (version 2)

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, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Pyxis 3D Titanium Cervical Cage System
Catalogue number Size Status
8062-1608S In distribution
8060-1608S In distribution
8071-0410S In distribution
GS166-7409P In distribution
8070-1210S In distribution
8070-0405S In distribution
8070-0409S In distribution
8071-1206S In distribution
8061-0810S In distribution
8061-0407S In distribution
8072-0006S In distribution
8062-0809S In distribution
8070-1609S In distribution
8060-0805S In distribution
8061-1210S In distribution
8072-1207S In distribution
8072-0005S In distribution
8061-0007S In distribution
8061-0807S In distribution
8061-0405S In distribution
8070-0806S In distribution
8060-0409S In distribution
8060-0806S In distribution
8060-0408S In distribution
8072-0405S In distribution
8060-0005S In distribution
8061-0410S In distribution
8062-0807S In distribution
8062-0806S In distribution
8062-1208S In distribution
8060-1210S In distribution
8072-1206S In distribution
8072-0810S In distribution
8070-0808S In distribution
8061-1209S In distribution
8072-0007S In distribution
8072-1608S In distribution
8061-0006S In distribution
8070-1206S In distribution
8072-1610S In distribution
8061-1607S In distribution
8062-1607S In distribution
8061-1207S In distribution
8071-0008S In distribution
8061-0805S In distribution
8062-0004S In distribution
8060-0807S In distribution
8071-1209S In distribution
8072-1209S In distribution
8062-0006S In distribution
8060-1610S In distribution
8071-0006S In distribution
8060-1208S In distribution
8060-1207S In distribution
8072-0808S In distribution
8070-0810S In distribution
8061-0008S In distribution
8060-0010S In distribution
8070-0410S In distribution
8060-0808S In distribution
8071-0007S In distribution
8060-0006S In distribution
8061-0409S In distribution
8062-1206S In distribution
8070-0809S In distribution
8072-1210S In distribution
GS166-8009P In distribution
8060-0007S In distribution
8071-0004S In distribution
8062-0810S In distribution
8061-1610S In distribution
8062-1609S In distribution
8060-0809S In distribution
GS166-8115P In distribution
8072-0010S In distribution
8070-0006S In distribution
8072-1208S In distribution
8072-0004S In distribution
8060-1209S In distribution
8062-0410S In distribution
8062-0005S In distribution
8071-0809S In distribution
8072-1609S In distribution
8070-0004S In distribution
8070-1207S In distribution
8062-0805S In distribution
8070-0007S In distribution
8071-0806S In distribution
8071-1208S In distribution
8062-0007S In distribution
8070-0807S In distribution
8070-0008S In distribution
8060-1609S In distribution
8070-0010S In distribution
8072-0807S In distribution
8072-0805S In distribution
8072-0409S In distribution
8070-0408S In distribution
8071-0009S In distribution
8071-1608S In distribution
8072-0407S In distribution
8071-0805S In distribution
8061-1206S In distribution
8060-0410S In distribution
8070-0406S In distribution
8061-0010S In distribution
8071-0808S In distribution
8071-0408S In distribution
8060-0810S In distribution
8060-0406S In distribution
8060-1607S In distribution
8071-0005S In distribution
8062-1610S In distribution
8060-0004S In distribution
8070-1607S In distribution
8070-1610S In distribution
8072-0410S In distribution
8071-1207S In distribution
8072-0408S In distribution
8062-1207S In distribution
8071-0406S In distribution
8070-1209S In distribution
8062-0408S In distribution
8061-0009S In distribution
8071-0405S In distribution
8062-0405S In distribution
8062-1209S In distribution
8060-0008S In distribution
8060-1206S In distribution
8060-0405S In distribution
8070-0005S In distribution
8072-0809S In distribution
8060-0009S In distribution
8062-0009S In distribution
8071-1607S In distribution
8070-1208S In distribution
8060-0407S In distribution
8061-0408S In distribution
8061-1208S In distribution
8070-0805S In distribution
8072-0806S In distribution
8070-0009S In distribution
8070-1608S In distribution
8061-1609S In distribution
8061-1608S In distribution
8071-0810S In distribution
8062-0010S In distribution
8061-0808S In distribution
8071-0010S In distribution
8072-0008S In distribution
8062-0008S In distribution
8072-0009S In distribution
8062-0409S In distribution
8061-0406S In distribution
8061-0806S In distribution
8071-1210S In distribution
8061-0004S In distribution
8071-0407S In distribution
8062-0407S In distribution
8071-1610S In distribution
8071-1609S In distribution
8062-0406S In distribution
8072-0406S In distribution
8061-0809S In distribution
8062-0808S In distribution
8062-1210S In distribution
8071-0409S In distribution
8070-0407S In distribution
8071-0807S In distribution
8072-1607S In distribution
8061-0005S 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
K223868 2023-04-26
K221687 2022-07-27
K131612 2014-04-18
K111354 2011-10-17

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