Concord

FORTRESS-Plus Radiopaque Bone Cement, 40g

Registry build 21.09.26
5manufacturers in China registered for this device type
5catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code NDN
Manufacturer City Province Registered as Device types
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai KiNETIC Medical Co Ltd Shanghai Shanghai Contract manufacturer 19
Ningbo Hicren Biotechnology Co., Ltd. Ningbo Zhejiang Manufacturer 5
Jieno Youcheng Medical Technology (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 3
Dragon Crown Medical Co., Ltd. Jinan Shandong Manufacturer 2

Record

Regulatory record for Concord
Listed by Globus Medical, Inc., United States
FDA product code NDN
Device type Cement, Bone, Vertebroplasty
Device class Class 2
Regulation 21 CFR 888.3027
Establishment Manufacturer, Exporter
510(k) K042168
Record published 2015-11-07
Record revised 2020-06-19 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Sizes Weight 20 to 40 g

Catalogue Numbers

Catalogue numbers for Concord
Catalogue number Size Status
4129.4000S Weight 40 g In distribution
458.693S In distribution
4129.4040S In distribution
4129.2000S Weight 20 g In distribution
4129.2020S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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Medinaut Plus Kyphoplasty System Imedicom Co., Ltd. 41
iVAS Stryker GmbH 35
V-Strut Vertebral Implant Hyprevention 28
Tracker Plus Kyphoplasty System GS Medical Co., Ltd. 25
StabiliT MX Fracture Kit Dfine, Inc. 12
Osseoflex® Merit Medical Systems, Inc. 8
Synth™ BES Imedicom Co., Ltd. 8
Tracker GS Medical Co., Ltd. 6
AVAflex Stryker GmbH 6

Showing 12 of 210. All products under Cement, Bone, Vertebroplasty

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K162618 2017-01-23
K042168 2005-01-14

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