Precept

PRECEPT Ti Rod, 110mm Prebent Lordotic

Registry build 21.09.26
14manufacturers in China registered for this device type
135catalogue numbers in this listing
21510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
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
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for Precept
Listed by Nuvasive, Inc., United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K102514
Record published 2019-12-04
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
8806530 In distribution
8847070 In distribution
8805540A In distribution
8828555 In distribution
8842300 In distribution
8847110 In distribution
8806530A In distribution
8895550 In distribution
8805540AP In distribution
8839555A In distribution
8848070 In distribution
8847180 In distribution
8847035P In distribution
8824535 In distribution
8897570 In distribution
8837020A In distribution
8847170 In distribution
8808550AP In distribution
8808590 In distribution
8896555 In distribution
8888550 In distribution
8808535A In distribution
8804560A In distribution
8888520 In distribution
8885530 In distribution
8808580AP In distribution
8889560 In distribution
8888525 In distribution
1675550 In distribution
8847120 In distribution
8848200P In distribution
8895060 In distribution
8808540A In distribution
8807580A In distribution
8895050 In distribution
8805550 In distribution
1677590 In distribution
8807530A In distribution
8896500 In distribution
8805535 In distribution
8834530B In distribution
8824545 In distribution
8888530 In distribution
8806560AP In distribution
8897050 In distribution
8886060 In distribution
1675545 In distribution
8848160 In distribution
8808535AP In distribution
8837545A In distribution
8839545A In distribution
8847200 In distribution
8809560A In distribution
8804550A In distribution
8839580A In distribution
8836590A In distribution
8841065 In distribution
8881035 In distribution
8886501 In distribution
8897045 In distribution
8847020 In distribution
8887090 In distribution
8896550 In distribution
8898530 In distribution
8896590 In distribution
8805560AP In distribution
8847140 In distribution
8847095P In distribution
8804525A In distribution
8889555 In distribution
8887002 In distribution
8837010A In distribution
8808580 In distribution
8898520 In distribution
8836550B In distribution
8836545B In distribution
8807580AP In distribution
8848500 In distribution
8847055 In distribution
8847035 In distribution
8808570 In distribution
8848100 In distribution
8895040 In distribution
8836530B In distribution
8897500 In distribution
8809545A In distribution
8885045 In distribution
8890545 In distribution
8848220P In distribution
8887025 In distribution
8888540 In distribution
8847140P In distribution
8898540 In distribution
8896510 In distribution
8848120 In distribution
8806540 In distribution
8807545AP In distribution
8835060B In distribution
8881090 In distribution
8830590A In distribution
8807545 In distribution
8895540 In distribution
8889500 In distribution
8886550 In distribution
8886055 In distribution
8804535AP In distribution
8847090P In distribution
8835025A In distribution
8847040P In distribution
8888560 In distribution
8836580B In distribution
8826535 In distribution
8809570AP In distribution
8898545 In distribution
8834540B In distribution
8848090 In distribution
8848200 In distribution
8836500A In distribution
8807570A In distribution
1677540 In distribution
8808590AP In distribution
8838535A In distribution
8807555AP In distribution
8884540 In distribution
8895035 In distribution
8836030A In distribution
8848500P In distribution
8836050B In distribution
8807540 In distribution
8847060 In distribution
8845500 In distribution
8838510A In distribution
8807560AP In distribution
8805555 In distribution
8848240P In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K131025 2013-11-27
K130868 2013-08-29
K122081 2013-02-01
K121815 2012-10-23
K121837 2012-07-16
K111866 2011-07-22
K111410 2011-06-20
K103750 2011-03-03
K093804 2010-02-19
K091071 2009-05-08
K083341 2009-03-20
K082070 2008-09-24
K073275 2008-01-29
K072339 2007-10-19
K071329 2007-08-08
K070148 2007-07-31
K070273 2007-04-03
K062590 2007-01-18
K061789 2006-08-10
K053581 2006-02-17
K041447 2004-08-16

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