AVS UniLIF

72 catalogue numbers from 48350074, listed by Stryker GmbH, Switzerland, 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
72catalogue numbers in this listing
17510(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 AVS UniLIF
Listed by Stryker GmbH, Switzerland
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2015-09-14
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, manufacturing date
Sizes Length 20 to 33 mm; angle 0 to 8 °; height 6 to 18 mm; width 8 to 11 mm

Catalogue Numbers

Catalogue numbers for AVS UniLIF
Catalogue number Size Status
48350074 Length 20.0 mm In distribution
48480104 Width 9.0 mm In distribution
48485154 Length 25.0 mm In distribution
48353084 Width 11.0 mm In distribution
48480130 Angle 0.0 ° In distribution
48390094 Width 11.0 mm In distribution
48390111 Height 11.0 mm In distribution
48395130 Height 13.0 mm In distribution
48351094 Angle 4.0 ° In distribution
48350064 Width 11.0 mm In distribution
48351130 Angle 0.0 ° In distribution
48390150 Length 20.0 mm In distribution
48353140 Length 33.0 mm In distribution
48485140 Length 25.0 mm In distribution
48351064 Angle 4.0 ° In distribution
48390120 Length 20.0 mm In distribution
48395114 Angle 4.0 ° In distribution
48353100 Length 33.0 mm In distribution
48353130 Width 11.0 mm In distribution
48485094 Angle 4.0 ° In distribution
48351060 Length 30.0 mm In distribution
48390090 Width 11.0 mm In distribution
48395100 Length 25.0 mm In distribution
48351070 Height 7.0 mm In distribution
48355070 Width 11.0 mm In distribution
48390128 Length 20.0 mm In distribution
48353124 Height 12.0 mm In distribution
48480074 Angle 4.0 ° In distribution
48395108 Angle 8.0 ° In distribution
48485114 Angle 4.0 ° In distribution
48353064 Length 33.0 mm In distribution
48485108 Height 10.0 mm In distribution
48351110 Height 11.0 mm In distribution
48355060 Height 6.0 mm In distribution
48485128 Angle 8.0 ° In distribution
48390164 Angle 4.0 ° In distribution
48353094 Height 9.0 mm In distribution
48390140 Height 14.0 mm In distribution
48395150 Angle 0.0 ° In distribution
48395098 Angle 8.0 ° In distribution
48485138 Angle 8.0 ° In distribution
48480084 Angle 4.0 ° In distribution
48353104 Width 11.0 mm In distribution
48395144 Angle 4.0 ° In distribution
48395104 Angle 4.0 ° In distribution
48480154 Angle 4.0 ° In distribution
48390130 Angle 0.0 ° In distribution
48480158 Height 15.0 mm In distribution
48351120 Length 30.0 mm In distribution
48485150 Height 15.0 mm In distribution
48395110 Height 11.0 mm In distribution
48480140 Width 9.0 mm In distribution
48395188 Width 11.0 mm In distribution
48390114 Length 20.0 mm In distribution
48351074 Length 30.0 mm In distribution
48390158 Height 15.0 mm In distribution
48480160 Angle 0.0 ° In distribution
48485148 Angle 8.0 ° In distribution
48480090 Length 20.0 mm In distribution
48353114 Length 33.0 mm In distribution
48395168 Angle 8.0 ° In distribution
48480124 Angle 4.0 ° In distribution
48351140 Height 14.0 mm In distribution
48485160 Angle 0.0 ° In distribution
48395164 Angle 4.0 ° In distribution
48351090 Width 11.0 mm In distribution
48351104 Height 10.0 mm In distribution
48390108 Height 10.0 mm In distribution
48395120 Length 25.0 mm In distribution
48395184 Length 25.0 mm In distribution
48480098 Height 9.0 mm In distribution
48390104 Height 10.0 mm 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
K200613 2020-04-15
K173476 2018-01-18
K162262 2016-11-09
K160955 2016-07-21
K160715 2016-07-08
K151726 2016-01-20
K152651 2015-12-15
K152304 2015-11-19
K143616 2015-03-05
K141217 2014-07-16
K093864 2010-03-11
K093704 2009-12-23
K090816 2009-04-24
K090166 2009-04-22
K083661 2009-02-27
K082014 2008-07-28
K080758 2008-03-27

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