SSE

SSE 5.2 TI Lock Screw F/Polyaxial Screw

Registry build 21.09.26
11manufacturers in China registered for this device type
45catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shandong (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWP
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
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
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Record

Regulatory record for SSE
Listed by Aesculap AG, Germany
FDA product code KWP
Device type Appliance, Fixation, Spinal Interlaminal
Device class Class 2
Regulation 21 CFR 888.3050
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-09-24
Record revised 2025-07-02 (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
Distribution end date 2016-02-18

Catalogue Numbers

Catalogue numbers for SSE
Catalogue number Size Status
SX101T Withdrawn
SX864T Diameter (mm) : 6.000 MM Withdrawn
SX251T Diameter (mm) : 5.000 MM Withdrawn
SX255T Length : 55.000 MM Withdrawn
SX853T Length : 45.000 MM Withdrawn
SX262T Diameter (mm) : 6.000 MM Withdrawn
SX264T Diameter (mm) : 6.000 MM Withdrawn
SX253T Diameter (mm) : 5.000 MM Withdrawn
SX294T Length : 50.000 MM Withdrawn
SX104T Diameter (mm) : 5.200 MM Withdrawn
SX004T Diameter (mm) : 15.000 MM Withdrawn
SX894T Diameter (mm) : 6.000 MM Withdrawn
SX252T Diameter (mm) : 5.000 MM Withdrawn
SX295T Diameter (mm) : 6.000 MM Withdrawn
SX298T Withdrawn
SX261T Length : 35.000 MM Withdrawn
SX860T Length : 30.000 MM Withdrawn
SX852T Length : 40.000 MM Withdrawn
SX299T Withdrawn
SX005T Diameter (mm) : 16.000 MM Withdrawn
SX895T Length : 55.000 MM Withdrawn
SX260T Diameter (mm) : 6.000 MM Withdrawn
SX865T Diameter (mm) : 6.000 MM Withdrawn
SX892T Diameter (mm) : 6.000 MM Withdrawn
SX263T Length : 45.000 MM Withdrawn
SX250T Length : 30.000 MM Withdrawn
SX291T Length : 35.000 MM Withdrawn
SX290T Diameter (mm) : 6.000 MM Withdrawn
SX292T Length : 40.000 MM Withdrawn
SX100T Withdrawn
SX893T Diameter (mm) : 6.000 MM Withdrawn
SX265T Diameter (mm) : 6.000 MM Withdrawn
SX862T Length : 40.000 MM Withdrawn
SX329T Withdrawn
SX850T Diameter (mm) : 5.000 MM Withdrawn
SX891T Diameter (mm) : 6.000 MM Withdrawn
SX293T Length : 45.000 MM Withdrawn
SX863T Diameter (mm) : 6.000 MM Withdrawn
SX026T Withdrawn
SX861T Diameter (mm) : 6.000 MM Withdrawn
SX851T Diameter (mm) : 5.000 MM Withdrawn
SX011T Withdrawn
SX854T Diameter (mm) : 5.000 MM Withdrawn
SX254T Diameter (mm) : 5.000 MM Withdrawn
SX704T Length : 40.000 MM Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Invictus Alphatec Spine, Inc. 5,422
ReLine Nuvasive, Inc. 4,439
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 3,188
Creo Globus Medical, Inc. 1,992
Apex Spine System Spinecraft LLC 1,319
LnK Spinal Fixation System L&K Biomed Co., Ltd. 1,271
Perla ® TL Spineart SA 1,035
Astra Spine System Spinecraft LLC 1,003
LineSider Highridge Medical, LLC 948
Apex-DL Spine System Spinecraft LLC 909
Revere Globus Medical, Inc. 875
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 841

Showing 12 of 536. All products under Appliance, Fixation, Spinal Interlaminal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K001080 2000-06-29
K980121 1998-06-10

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