BN Cage

Medyssey PEEK Lumbar Cage, 22mm Length, 9mm Width, 14mm Height, 0-degrees Lordosis

Registry build 21.09.26
14manufacturers in China registered for this device type
105catalogue 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 BN Cage
Listed by Medyssey 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
Record published 2016-09-12
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
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for BN Cage
Catalogue number Size Status
BS01422 In distribution
BS41132 In distribution
BS81432 In distribution
BS81030 In distribution
BS41527 In distribution
BS01322 In distribution
BS01232 In distribution
BS01530 In distribution
BS01522 In distribution
BS81332 In distribution
BS41532 In distribution
BS81022 In distribution
BS00932 In distribution
BS40932 In distribution
BS41122 In distribution
BS41127 In distribution
BS41332 In distribution
BS41427 In distribution
BS01125 In distribution
BS41525 In distribution
BS01532 In distribution
BS01525 In distribution
BS41222 In distribution
BS40930 In distribution
BS40922 In distribution
BS81122 In distribution
BS01132 In distribution
BS01222 In distribution
BS00925 In distribution
BS81330 In distribution
BS01130 In distribution
BS00822 In distribution
BS00927 In distribution
BS81025 In distribution
BS81132 In distribution
BS01030 In distribution
BS41327 In distribution
BS81532 In distribution
BS81232 In distribution
BS01325 In distribution
BS81527 In distribution
BS01127 In distribution
BS81027 In distribution
BS01230 In distribution
BS41422 In distribution
BS81125 In distribution
BS81522 In distribution
BS81130 In distribution
BS81425 In distribution
BS81427 In distribution
BS01427 In distribution
BS41227 In distribution
BS01032 In distribution
BS41025 In distribution
BS01027 In distribution
BS00830 In distribution
BS01330 In distribution
BS81032 In distribution
BS81327 In distribution
BS01332 In distribution
BS00922 In distribution
BS41130 In distribution
BS81127 In distribution
BS41430 In distribution
BS41432 In distribution
BS41032 In distribution
BS81430 In distribution
BS01430 In distribution
BS41325 In distribution
BS41125 In distribution
BS41230 In distribution
BS01327 In distribution
BS41232 In distribution
BS81325 In distribution
BS01122 In distribution
BS81322 In distribution
BS01527 In distribution
BS81222 In distribution
BS00832 In distribution
BS81530 In distribution
BS41022 In distribution
BS81230 In distribution
BS01022 In distribution
BS41330 In distribution
BS81422 In distribution
BS00827 In distribution
BS00825 In distribution
BS01227 In distribution
BS01225 In distribution
BS81227 In distribution
BS40925 In distribution
BS01432 In distribution
BS81225 In distribution
BS40927 In distribution
BS01025 In distribution
BS01425 In distribution
BS41322 In distribution
BS00930 In distribution
BS41425 In distribution
BS81525 In distribution
BS41027 In distribution
BS41225 In distribution
BS41522 In distribution
BS41030 In distribution
BS41530 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
K121246 2012-06-15
K110067 2011-04-08

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