Mectalif Anterior Implants

MectaLIF Anterior Stand-alone Screw Diam.5.5x30 Long Head (2x)

Registry build 21.09.26
3manufacturers in China registered for this device type
16catalogue numbers in this listing
2510(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 Mectalif Anterior Implants
Listed by Medacta International SA, Switzerland
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer, Exporter
510(k) K183426
Record published 2019-03-20
Record revised 2024-09-11 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Mectalif Anterior Implants
Catalogue number Size Status
03.30.145 In distribution
03.30.152 In distribution
03.30.147 In distribution
03.30.156 In distribution
03.30.141 In distribution
03.30.143 In distribution
03.30.153 In distribution
03.30.148 In distribution
03.30.142 In distribution
03.30.155 In distribution
03.30.157 In distribution
03.30.146 In distribution
03.30.154 In distribution
03.30.151 In distribution
03.30.144 In distribution
03.30.158 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
K160605 2016-07-21
K124034 2013-05-17

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