Pass TL

ILIAC CLOSED SCREW Ø6,5 mm x 75 mm

Registry build 21.09.26
15manufacturers in China registered for this device type
40catalogue numbers in this listing
9510(k) clearances naming this product code
2recalls 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 Pass TL
Listed by Medicrea International, France
FDA product code NKB
Device type Thoracolumbosacral Pedicle Screw System
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Specification developer, Manufacturer
510(k) K162786
Record published 2017-12-13
Record revised 2025-07-02 (version 7)

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, expiry date
Distribution end date 2023-03-24
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Pass TL
Catalogue number Size Status
B22110010 In distribution
B22110008 In distribution
B22110001 In distribution
B22111508R In distribution
B22110009 In distribution
B22120006 In distribution
B22111510R In distribution
B22111510L In distribution
B22111508L In distribution
B22111509L In distribution
B22120005 In distribution
B22120008 In distribution
B22111509R In distribution
B22026570 Withdrawn
B22006545 Withdrawn
B22046575 Withdrawn
B22005535 Withdrawn
B22004555 Withdrawn
B22005550 Withdrawn
B22004525 Withdrawn
B22000040 Withdrawn
B22007540 Withdrawn
B22004535 Withdrawn
B22004540 Withdrawn
B22004545 Withdrawn
B22026575 Withdrawn
B22026565 Withdrawn
B22004560 Withdrawn
B22046580 Withdrawn
B22005525 Withdrawn
B22006535 Withdrawn
B22046570 Withdrawn
B22005540 Withdrawn
B22005545 Withdrawn
B22006540 Withdrawn
B22007530 Withdrawn
B22026580 Withdrawn
B22004550 Withdrawn
B22004530 Withdrawn
B22006550 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
K220724 2022-04-08
K213281 2022-01-05
K190376 2019-05-02
K182240 2018-10-17
K162786 2017-01-25
K160640 2016-09-23
K161627 2016-07-29
K153413 2016-04-22
K141398 2015-01-09

Recalls

2 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
2019-11-11 Class II Device Design Incompatible universal counter torque (A22020500) with the nut driver T30 (A22020220) 3 units 2020-10-14
2019-06-27 Class II Employee error It has been determined that some Pedicle system screw identified as 45mm long have an actual length of 50mm. Pedicle screws with a diameter of 7.5 mm or more are reserved for the sacrum area. As a result, a screw that is too long could com 210 Pedicle Screws 2020-11-19

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