MAS PCF

MAS PCF Screw, 3.5x36mm

Registry build 21.09.26
11manufacturers in China registered for this device type
20catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shandong (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWP
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Record

Regulatory record for MAS PCF
Listed by Nuvasive, Inc., United States
FDA product code KWP
Device type Appliance, Fixation, Spinal Interlaminal
Device class Class 2
Regulation 21 CFR 888.3050
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K150474
Record published 2016-08-02
Record revised 2025-06-11 (version 6)

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

Catalogue Numbers

Catalogue numbers for MAS PCF
Catalogue number Size Status
8945336 In distribution
8945326 In distribution
8945720 In distribution
8945316 In distribution
8945318 In distribution
8945434 In distribution
8945436 In distribution
8945314 In distribution
8945724 In distribution
8945708 In distribution
8945412 In distribution
8945426 In distribution
8945728 In distribution
8945732 In distribution
8945432 In distribution
8945718 In distribution
8945334 In distribution
8945736 In distribution
8945430 In distribution
8945726 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Invictus Alphatec Spine, Inc. 5,422
ReLine Nuvasive, Inc. 4,439
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 3,188
Creo Globus Medical, Inc. 1,992
Apex Spine System Spinecraft LLC 1,319
LnK Spinal Fixation System L&K Biomed Co., Ltd. 1,271
Perla ® TL Spineart SA 1,035
Astra Spine System Spinecraft LLC 1,003
LineSider Highridge Medical, LLC 948
Apex-DL Spine System Spinecraft LLC 909
Revere Globus Medical, Inc. 875
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 841

Showing 12 of 536. All products under Appliance, Fixation, Spinal Interlaminal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K093319 2010-06-23
K073278 2008-03-28

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