Audere Posterior Lumbar Spacer System

THE Audere Posterior Lumbar Spacer System Consists OF Implants, Trials AND Instruments. THE Audere Lumbar Spacer System MAY BE Implanted Bilaterally Using A Posterior (Plif) Approach, OR AS…

Registry build 21.09.26

THE Audere Posterior Lumbar Spacer System Consists OF Implants, Trials AND Instruments. THE Audere Lumbar Spacer System MAY BE Implanted Bilaterally Using A Posterior (Plif) Approach, OR AS A Single Device Employing A Transforaminal (Tlif) Approach.

14manufacturers in China registered for this device type
58catalogue numbers in this listing
1510(k) clearance

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 Audere Posterior Lumbar Spacer System
Listed by Met 1 Technologies, LLC, 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) K160699
Record published 2017-05-29
Record revised 2020-02-24 (version 4)

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, serial number
Sizes Length 7 to 25 mm; height 7 to 14 mm

Catalogue Numbers

Catalogue numbers for Audere Posterior Lumbar Spacer System
Catalogue number Size Status
10251100 Length 25 mm In distribution
30290203 In distribution
10201400 Length 20 mm In distribution
30290131 In distribution
30290110 In distribution
30290101 In distribution
10250900 Length 25 mm In distribution
10250700 Length 25 mm In distribution
30290133 In distribution
30290146 In distribution
30290105 In distribution
30290106 In distribution
10200700 Length 20 mm In distribution
30290107 In distribution
30290205 Length 8 mm In distribution
10251400 Length 25 mm In distribution
30290135 In distribution
30290148 In distribution
30290129 In distribution
30290103 In distribution
10251200 Length 25 mm In distribution
30290141 In distribution
10251300 Length 25 mm In distribution
30290132 In distribution
30290112 In distribution
30290137 In distribution
30290140 In distribution
30290207 Length 10 mm In distribution
10201000 Length 20 mm In distribution
30290109 In distribution
30290209 In distribution
10201300 Length 20 mm In distribution
30290149 In distribution
10200800 Length 20 mm In distribution
30290111 In distribution
30290153 In distribution
30290150 In distribution
30290152 In distribution
10251000 Length 25 mm In distribution
30290138 In distribution
30290108 In distribution
30290130 In distribution
30290134 In distribution
30290139 In distribution
30290151 In distribution
30290142 In distribution
30290104 In distribution
30290204 Length 7 mm In distribution
30290202 In distribution
30290147 In distribution
30290206 Length 9 mm In distribution
10201200 Length 20 mm In distribution
10250800 Length 25 mm In distribution
30290154 In distribution
10200900 Length 20 mm In distribution
10201100 Length 20 mm In distribution
30290136 In distribution
30290102 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
K160699 2016-08-01

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