Invictus OsseoScrew

Invictus OsseoScrew is a pedicle-screw system with a titanium-alloy core and an expandable shank made from commercially pure titanium. Its cannulated polyaxial screws connect with…

Registry build 21.09.26

Invictus OsseoScrew is a pedicle-screw system with a titanium-alloy core and an expandable shank made from commercially pure titanium. Its cannulated polyaxial screws connect with compatible Invictus spinal fixation components.

The screws are available in 6.5 and 7.5 mm diameters and lengths from 40 to 55 mm. Associated instruments support placement, while compatible rods and connectors complete the spinal construct.

Listed Item

Invictus OsseoScrew Ratcheting Egg Handle, Cannulated

Fixation Context

This configuration is intended to restore spinal-column integrity for a limited period in patients with advanced thoracic or lumbar tumors whose expected survival is insufficient to achieve fusion. It is used with the Invictus Spinal Fixation System and the specified Invictus CT transition rods.

15manufacturers in China registered for this device type
40catalogue numbers in this listing
20510(k) clearances naming this product code
5recalls 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 Invictus OsseoScrew
Listed by Alphatec Spine, 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) K202327
Record published 2021-02-06
Record revised 2024-09-11 (version 4)

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
Sizes Outer diameter 6.5 to 7.5 mm; length 40 to 55 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Invictus OsseoScrew
Catalogue number Size Status
15905-065-050 Outer Diameter 6.5 mm In distribution
15925-075-050 Length 50 mm In distribution
15905-065-045 Length 45 mm In distribution
15905-075-050 Outer Diameter 7.5 mm In distribution
15915-075-050 Length 50 mm In distribution
17901 In distribution
15915-065-050 Outer Diameter 6.5 mm In distribution
15915-065-040 Length 40 mm In distribution
16196-050 In distribution
15915-075-055 Length 55 mm In distribution
15915-065-055 Outer Diameter 6.5 mm In distribution
15925-075-040 Length 40 mm In distribution
15925-075-055 Length 55 mm In distribution
16196-040 In distribution
15915-065-045 Length 45 mm In distribution
16184 In distribution
15905-075-045 Length 45 mm In distribution
15915-075-045 Outer Diameter 7.5 mm In distribution
15925-065-055 Outer Diameter 6.5 mm In distribution
16180 In distribution
15905-075-055 Length 55 mm In distribution
16183-040 In distribution
15925-065-040 Outer Diameter 6.5 mm In distribution
15915-075-040 Length 40 mm In distribution
17814-055 In distribution
15905-075-040 Outer Diameter 7.5 mm In distribution
15905-065-055 Length 55 mm In distribution
15925-065-050 Length 50 mm In distribution
16196-045 In distribution
15925-075-045 Length 45 mm In distribution
15905-065-040 Length 40 mm In distribution
17904 In distribution
16183-050 In distribution
16183-045 In distribution
17814-040 In distribution
17814-045 In distribution
17814-050 In distribution
16183-055 In distribution
15925-065-045 Outer Diameter 6.5 mm In distribution
16196-055 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
K261284 2026-07-14
K241519 2024-06-21
K232275 2023-09-27
K214006 2022-04-04
K213460 2021-12-10
K203056 2020-11-23
K202327 2020-10-15
K192938 2019-12-12
K181980 2018-09-25
K181677 2018-08-09
K173522 2017-11-30
K161363 2016-06-10
K152968 2015-12-30
K143149 2015-01-05
K133221 2014-03-13
K131119 2013-05-21
K123623 2013-02-14
K111634 2012-01-25
K111076 2011-07-12
K071380 2007-08-20

Recalls

5 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
2017-05-05 Class II Under Investigation by firm Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due to a trend in set screw
postoperative disengagement from the screw body.
16,959 units 2017-06-06
2016-10-05 Class II Under Investigation by firm Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due to a trend in set screw postoperative disengagement from the screw body. 16,972 units 2017-02-17
2014-06-26 Class II Unknown/Undetermined by firm Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they received a report that the instrument malfunctioned and golden stop slid from its fixed position during use. 14 units total (12 units in US) 2014-09-03
2013-06-28 Class II Equipment maintenance The firm initiated this recall of certain lots of Illico Ti Cannulated Polyaxial Screws 7.5mm x 40mm implants, due to an off-center cannulation hole at the proximal end of the bone screw. There is a potential risk that when the screw is mat 333 screws 2014-10-09
2013-05-06 Class II Device Design Alphatec Spine initiated this medical device recall for the following reason: due to tolerancing, the flange of the Phygen Leucadia” Autolok set screw may interfere with the top of the screw head prior to fully locking the rod. If this cond 1,814 2014-09-25

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