Response Spine 5.5/6.0 System

5.5/6.0 Polyaxial Reduction Pedicle Screws - Ø5.5mm, 30mm Length

Registry build 21.09.26
7manufacturers in China registered for this device type
52catalogue numbers in this listing
3510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (4), Shandong (2), Shanghai (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OSH
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
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

Record

Regulatory record for Response Spine 5.5/6.0 System
Listed by Orthopediatrics, Corp, United States
FDA product code OSH
Device type Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K150600
Record published 2015-06-30
Record revised 2025-04-11 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
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
00-1300-0435 In distribution
00-1300-9530 In distribution
00-1300-6435 In distribution
00-1300-1550 In distribution
00-1300-2965 In distribution
00-1300-2540 In distribution
00-1300-8655 In distribution
00-1300-1425 In distribution
00-1300-3911 In distribution
00-1300-8625 In distribution
00-1300-7530 In distribution
00-1300-1680 In distribution
00-1300-2725 In distribution
00-1300-0525 In distribution
00-1300-6655 In distribution
00-1300-8550 In distribution
00-1300-9430 In distribution
00-1300-6550 In distribution
00-1300-3045 In distribution
00-1300-3811 In distribution
00-1300-2855 In distribution
00-1300-2530 In distribution
00-1300-3012 In distribution
00-1300-0620 In distribution
00-1300-6555 In distribution
00-1300-6685 In distribution
00-1300-2865 In distribution
00-1300-2710 In distribution
00-1300-7440 In distribution
00-1300-2960 In distribution
00-1300-7640 In distribution
00-1300-7430 In distribution
00-1300-2660 In distribution
00-1300-6440 In distribution
00-1300-7540 In distribution
00-1300-1535 In distribution
00-1300-9645 In distribution
00-1300-3075 In distribution
00-1300-9620 In distribution
00-1300-3041 In distribution
00-1300-0635 In distribution
00-1300-8685 In distribution
00-1300-7425 In distribution
00-1300-2950 In distribution
00-1300-8660 In distribution
00-1300-7665 In distribution
00-1300-0770 In distribution
00-1300-1670 In distribution
00-1300-8520 In distribution
00-1300-6680 In distribution
00-1300-9440 In distribution
00-1300-2435 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Creo Globus Medical, Inc. 1,821
ReLine Nuvasive, Inc. 1,093
Olympic Astura Medical 951
Nex-D2 Next Orthosurgical 887
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 876
Arsenal Alphatec Spine, Inc. 820
Apex-DL Spine System Spinecraft LLC 691
Polaris™ 4.75 Spinal System Biomet Spine 413
Expedium Medos International Sàrl 400
Implanet Spine System Implanet 386
Everest® Spinal System VB Spine LLC 299
Arsenal Deformity Spinal Fixation System Alphatec Spine, Inc. 258

Showing 12 of 73. All products under Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K130655 2013-05-08
K121250 2012-06-19
K120291 2012-04-16

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