Response Spine 5.5/6.0 System

5.5/6.0 Polyaxial Reduction Pedicle Screws - Ø6.5mm, 65mm Length

Registry build 21.09.26
11manufacturers in China registered for this device type
52catalogue numbers in this listing

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 Response Spine 5.5/6.0 System
Listed by Orthopediatrics, Corp, United States
FDA product code KWP
Device type Appliance, Fixation, Spinal Interlaminal
Device class Class 2
Regulation 21 CFR 888.3050
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K150600
Record published 2016-10-14
Record revised 2025-04-11 (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, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Response Spine 5.5/6.0 System
Catalogue number Size Status
00-1300-6425 In distribution
00-1300-7680 In distribution
00-1300-6530 In distribution
00-1300-2670 In distribution
00-1300-2770 In distribution
00-1300-3151 In distribution
00-1300-2850 In distribution
00-1300-2560 In distribution
00-1300-2750 In distribution
00-1300-6540 In distribution
00-1300-0425 In distribution
00-1300-2665 In distribution
00-1300-1530 In distribution
00-1300-6520 In distribution
00-1300-1730 In distribution
00-1300-7570 In distribution
00-1300-0630 In distribution
00-1300-2565 In distribution
00-1300-8565 In distribution
00-1300-1655 In distribution
00-1300-2420 In distribution
00-1300-0790 In distribution
00-1300-0670 In distribution
00-1300-2975 In distribution
00-1300-0760 In distribution
00-1300-1565 In distribution
00-1300-7525 In distribution
00-1300-2955 In distribution
00-1300-0650 In distribution
00-1300-1750 In distribution
00-1300-0555 In distribution
00-1300-2880 In distribution
00-1300-8535 In distribution
00-1300-0640 In distribution
00-1300-2735 In distribution
00-1300-8440 In distribution
00-1300-9665 In distribution
00-1300-1780 In distribution
00-1300-7635 In distribution
00-1300-7555 In distribution
00-1300-2070 In distribution
00-1300-7435 In distribution
00-1300-9575 In distribution
00-1300-2912 In distribution
00-1300-0755 In distribution
00-1300-3050 In distribution
00-1300-0740 In distribution
00-1300-1710 In distribution
00-1300-1435 In distribution
00-1300-1540 In distribution
00-1300-0780 In distribution
00-1300-8665 In distribution

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

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Response Spine 5.5/6.0 System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Orthopediatrics, Corp 510(k) number 2020-07-06 Class II Under Investigation by firm Product may have incorrect laser etched alignment lines, the non-conforming laser etch may have compromised strength, lead to unintended fracture of the device 73 units
Orthopediatrics, Corp 510(k) number 2017-08-03 Class II Employee error The 7mm diameter uniaxial pedicle screws have been color anodized with the same color utilized on 5 mm diameter screws. 24 units 2019-05-08
Orthopediatrics, Corp 510(k) number 2015-11-10 Class II Process change control Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have been manufactured incorrectly, thus preventing the driver from fully engaging into the hexagonal drive feature of the screw. 102 2016-05-23

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