AVS Navigator

18 catalogue numbers from 48393130, listed by Stryker GmbH, Switzerland, under Intervertebral Fusion Device With Integrated Fixation, Lumbar. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
18catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OVD
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for AVS Navigator
Listed by Stryker GmbH, Switzerland
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, 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 Height 6 to 15 mm; length 26 to 31 mm; angle 0 to 4 °

Catalogue Numbers

Catalogue numbers for AVS Navigator
Catalogue number Size Status
48393130 Height 13.0 mm In distribution
48393124 Angle 4.0 ° In distribution
48393070 Length 31.0 mm In distribution
48392110 Angle 0.0 ° In distribution
48393110 Height 11.0 mm In distribution
48392104 Height 10.0 mm In distribution
48393060 Height 6.0 mm In distribution
48392140 Length 26.0 mm In distribution
48392100 Angle 0.0 ° In distribution
48393080 Height 8.0 mm In distribution
48392124 Length 26.0 mm In distribution
48392084 Angle 4.0 ° In distribution
48393094 Length 31.0 mm In distribution
48392150 Angle 0.0 ° In distribution
48392154 Length 26.0 mm In distribution
48393140 Length 31.0 mm In distribution
48392064 Height 6.0 mm In distribution
48393154 Height 15.0 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sirion Astura Medical 1,465
IdentiTi Alphatec Spine, Inc. 1,372
EL Capitan Astura Medical 1,205
Zavation Zavation 1,157
Brigade Nuvasive, Inc. 1,005
Solar™ Interbody Fusion System Degen Medical 899
Zavation F3D Corpectomy Zavation 730
ROI-A Ldr Spine USA 552
Avenue L Ldr Spine USA 524
Transcend Nanotec Alphatec Spine, Inc. 485
Endoskeleton® TL Hyperlordotic nanoLOCK® Surface Technology Titan Spine, LLC 462
Base Nuvasive, Inc. 462

Showing 12 of 241. All products under Intervertebral Fusion Device With Integrated Fixation, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201585 2020-08-10
K143163 2015-01-26
K142066 2014-11-13
K133328 2014-05-30

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