MAS Plif

MAS PLIF Screw, 5.0 x 30mm Polyaxial 3Z

Registry build 21.09.26
15manufacturers in China registered for this device type
23catalogue numbers in this listing
9510(k) clearances naming this product code
31recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Shandong (3). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NKB
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
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
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
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
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

Showing 12 of 15. All 15 manufacturers in China registered for Thoracolumbosacral Pedicle Screw System

Record

Regulatory record for MAS Plif
Listed by Nuvasive, Inc., United States
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K062317
Record published 2015-10-24
Record revised 2025-06-11 (version 10)

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 Plif
Catalogue number Size Status
7242045 In distribution
7075535 In distribution
7242080 In distribution
1595040 In distribution
7242090 In distribution
7242095 In distribution
7096525 In distribution
7095550 In distribution
7885030 In distribution
7095050 In distribution
1616025 In distribution
7070000 In distribution
7242020 In distribution
1596030 In distribution
1595535 In distribution
7884540 In distribution
7242110 In distribution
1594520 In distribution
7242040 In distribution
7094540 In distribution
7242070 In distribution
7124540 In distribution
7094530 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
The Jasper Spinal Fixation System Gbs Commonwealth Co., Ltd. 32,491
Invictus Alphatec Spine, Inc. 4,722
Vital Spinal Fixation System Highridge Medical, LLC 4,422
Innoverse Spinal System CG MedTech Co., Ltd. 4,240
4CIS® Chiron Spinal Fixation System Alpha AI Co., Ltd. 3,787
LnK Spinal Fixation System L&K Biomed Co., Ltd. 3,522
Hedjet System Medyssey Co., Ltd. 3,438
Anax™ 5.5 Spinal System CG MedTech Co., Ltd. 3,424
Mega Plus MIS Spine System BK Meditech Co., Ltd. 3,396
ReLine Nuvasive, Inc. 2,882
Nex-D2 Next Orthosurgical 2,765
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 2,386

Showing 12 of 1,490. All products under Thoracolumbosacral Pedicle Screw System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K132014 2013-10-31
K122352 2012-09-11
K121619 2012-08-24
K102514 2010-12-01
K092287 2009-10-06
K091502 2009-07-22
K090981 2009-07-02
K083028 2008-11-13
K082332 2008-10-10

Recalls

31 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19
2009-01-05 Class II Device Design The tulip portion of the screw assembly can disengage from the shank after implantation. 240 units total 2012-11-19

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