Precept

PRECEPT Screw, 10.5x100mm Polyaxial C.R.

Registry build 21.09.26
15manufacturers in China registered for this device type
133catalogue 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 Precept
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) K171894
Record published 2019-12-09
Record revised 2025-06-11 (version 6)

Specifications

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

Catalogue Numbers

Catalogue numbers for Precept
Catalogue number Size Status
8847065P In distribution
8806535AP In distribution
8886545 In distribution
8806545AP In distribution
8808545AP In distribution
8806535A In distribution
8804540AP In distribution
8836510B In distribution
8885560 In distribution
8830520A In distribution
8837030A In distribution
8848180 In distribution
8848170P In distribution
8805535A In distribution
8830545A In distribution
8881080 In distribution
8847045 In distribution
8830525A In distribution
8836580A In distribution
8837035A In distribution
8896520 In distribution
8847075P In distribution
8805555A In distribution
8807570AP In distribution
8836060B In distribution
8837050A In distribution
8886560 In distribution
8836520A In distribution
8809500AP In distribution
8809570A In distribution
8808590A In distribution
8807540AP In distribution
8890555 In distribution
8895025 In distribution
8881012 In distribution
8845500P In distribution
8847085 In distribution
8847080P In distribution
8847070P In distribution
8835545B In distribution
8888510 In distribution
8809550A In distribution
8837510A In distribution
8848230P In distribution
8841060 In distribution
8836500B In distribution
8885550 In distribution
8885555 In distribution
8807540A In distribution
8848210P In distribution
8808500AP In distribution
8885535 In distribution
1676550 In distribution
8885545 In distribution
8804555A In distribution
8847030P In distribution
8834535A In distribution
8809500A In distribution
8839530A In distribution
8837500A In distribution
8815550 In distribution
8895535 In distribution
8809580A In distribution
8835045B In distribution
8809555A In distribution
8887000 In distribution
8839510A In distribution
8807545A In distribution
8827535 In distribution
8807590AP In distribution
8836540B In distribution
8805530AP In distribution
8899545 In distribution
8848240 In distribution
8807530 In distribution
8887001 In distribution
8837570A In distribution
8836045A In distribution
8848250P In distribution
8808570A In distribution
8841020 In distribution
8848140 In distribution
8839550A In distribution
8837590A In distribution
8835030B In distribution
8885025 In distribution
8808550A In distribution
8807555 In distribution
8886570 In distribution
8838580A In distribution
8837520A In distribution
8807590A In distribution
8809540A In distribution
8836525A In distribution
8847130 In distribution
8836555B In distribution
8886045 In distribution
8807550AP In distribution
8847120P In distribution
8885030 In distribution
8848160P In distribution
8804530A In distribution
8809580AP In distribution
8837090A In distribution
1675540 In distribution
8836060A In distribution
8805540 In distribution
8807535AP In distribution
8806550A In distribution
8887535 In distribution
8898590 In distribution
8808555A In distribution
8839540A In distribution
8894530 In distribution
8835535B In distribution
8848050 In distribution
8838545A In distribution
8838560A In distribution
8889525 In distribution
8808500A In distribution
8839570A In distribution
8839560A In distribution
8804525AP In distribution
8885035 In distribution
8800500A In distribution
8830540A In distribution
8807550A In distribution
8848190P In distribution
8808530A In distribution
8848180P In distribution
8835025B In distribution
8836560A In distribution
8881060 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