Quantum™* Spinal Fixation System

75 catalogue numbers from 10-55-PR-140, listed by Pioneer Surgical Technology, Inc., United States, under Thoracolumbosacral Pedicle Screw System. 15 manufacturers in China are registered for this product code.

Registry build 21.09.26
15manufacturers in China registered for this device type
75catalogue numbers in this listing
13510(k) clearances naming this product code
3recalls 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 Quantum™* Spinal Fixation System
Listed by Pioneer Surgical Technology, Inc., United States
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Record published 2015-11-23
Record revised 2025-07-02 (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
Distribution end date 2023-05-22

Catalogue Numbers

Catalogue numbers for Quantum™* Spinal Fixation System
Catalogue number Size Status
10-55-PR-140 Withdrawn
10-PJC5002070-L Withdrawn
10-TLH-L Withdrawn
10-PJC5001050-R 5.5mm X 500mm X 10mm X 50mm Withdrawn
10-LHO-L Withdrawn
10-PJC5001060-L 5.5mm X 500mm X 10mm X 60mm Withdrawn
10-PJC5003070-R 5.5mm X 500mm X 30mm X 70mm Withdrawn
10-475-PA-45 Withdrawn
10-575-FX-30 Withdrawn
10-PJC5003050-L 5.5mm X 500mm X 30mm X 50mm Withdrawn
10-475-PA-30 4.75mm (D) X 30mm (L) Withdrawn
10-875-FX-65 8.75mm (D) X 65mm (L) Withdrawn
10-55-PR-55 Withdrawn
10-16-FXL Withdrawn
10-475-PA-50 4.75mm (D) X 50mm (L) Withdrawn
10-400-PA-40 4.00mm (D) X 40mm (L) Withdrawn
10-575-FX-35 Withdrawn
10-12-FXL 12mm Withdrawn
10-475-FX-35 Withdrawn
10-55-RR-60 Withdrawn
10-675-PAT-50 6.75mm (D) X 50mm (L) Withdrawn
10-675-PA-50 Withdrawn
10-55-RR-110 Withdrawn
10-LHO-R Withdrawn
10-PJC5002060-L 5.5mm X 500mm X 20mm X 60mm Withdrawn
10-400-PA-20 Withdrawn
10-675-PA-30 Withdrawn
10-775-PA-90 Withdrawn
10-55-PR-145 Withdrawn
10-PJC5001070-R 5.5mm X 500mm X 10mm X 70mm Withdrawn
10-RCPM 5.5mm X 6.35mm Withdrawn
10-55-PR-70 Withdrawn
10-775-PA-100 Withdrawn
10-55-RR-70 Withdrawn
10-675-PA-90 6.75mm (D) X 90mm (L) Withdrawn
10-15-FXL 15mm Withdrawn
10-RCPM Withdrawn
10-400-FX-45 Withdrawn
10-LOC-60 60mm Withdrawn
10-15-FXL Withdrawn
10-RCP Withdrawn
10-775-FX-35 Withdrawn
10-12-FXL Withdrawn
10-775-PA-65 7.75mm (D) X 65mm (L) Withdrawn
10-675-PAT-35 6.75mm (D) X 35mm (L) Withdrawn
10-875-FX-100 8.75mm (D) X 100mm (L) Withdrawn
10-675-FX-50 Withdrawn
10-400-FX-40 Withdrawn
10-LLHE-L Withdrawn
10-14-FXL 14mm Withdrawn
10-PJC5003080-R 5.5mm X 500mm X 30mm X 80mm Withdrawn
10-55-RHC-600 Withdrawn
10-PJC5003050-R Withdrawn
10-675-PA-25 Withdrawn
10-55-RR-40 Withdrawn
10-400-FX-20 Withdrawn
10-875-FX-50 8.75mm (D) X 50mm (L) Withdrawn
10-7080-VXL Withdrawn
10-775-FX-45 Withdrawn
10-LOC-30 Withdrawn
10-LOC-30 30mm Withdrawn
10-875-FX-75 Withdrawn
10-5060-VXL Withdrawn
10-675-PA-30 6.75mm (D) X 30mm (L) Withdrawn
10-775-PA-80 Withdrawn
10-675-FX-35 6.75mm (D) X 35mm (L) Withdrawn
10-500-PA-40 5.00mm (D) X 40mm (L) Withdrawn
10-575-PA-35 Withdrawn
10-PJC5003070-L Withdrawn
10-775-PA-50 7.75mm (D) X 50mm (L) Withdrawn
10-775-PA-45 Withdrawn
10-RCEM Withdrawn
10-775-FX-40 7.75mm (D) X 40mm (L) Withdrawn
10-675-PA-80 Withdrawn
10-400-PA-50 4.00mm (D) X 50mm (L) Withdrawn

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
K192396 2019-11-26
K140696 2014-04-10
K131100 2013-06-27
K130286 2013-04-01
K111502 2011-08-23
K110692 2011-05-12
K101790 2011-03-07
K093692 2010-08-11
K080504 2008-03-20
K080518 2008-03-20
K070973 2007-07-03
K070551 2007-03-29
K041167 2004-07-23

Recalls

1 of these is 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
2013-06-14 Class II Device Design The affected fixed rod holders did not allow the instrument to lock down on the spinal rod. 9 2014-09-30
2005-07-29 Not classified Other Screw may be incorrectly etched as to length. 124 2005-10-25
2005-07-29 Not classified Other Screw may be incorrectly etched as to length. 110 2005-10-25

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