Concerto Detachable Coil System

Coil PV-14-30-HELIX V07

Registry build 21.09.26
6manufacturers in China registered for this device type
44catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (4), Guangdong (1), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KRD
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3
Microport Neurotech (Shanghai) Co., Ltd. Shanghai Shanghai Manufacturer 2
Suzhou Haowei Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 1

Record

Regulatory record for Concerto Detachable Coil System
Listed by Micro Therapeutics, Inc., United States
FDA product code KRD
Device type Device, Vascular, For Promoting Embolization
Device class Class 2
Regulation 21 CFR 870.3300
510(k) K090046
Record published 2022-06-04
Record revised 2024-09-25 (version 3)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Storage Storage environment temperature up to 50 °C; Special storage condition: store in a cool dry place
Distribution end date 2023-08-30

Catalogue Numbers

Catalogue numbers for Concerto Detachable Coil System
Catalogue number Size Status
PV-9-30-3D In distribution
NV-2-4-HELIX In distribution
PV-3-4-3D In distribution
PV-14-30-HELIX In distribution
NV-2-8-HELIX In distribution
PV-8-30-3D In distribution
PV-6-20-3D In distribution
PV-4-10-3D In distribution
NV-9-30-HELIX In distribution
NV-2-6-HELIX In distribution
PV-10-30-3D In distribution
NV-5-20-HELIX In distribution
PV-16-40-HELIX In distribution
PV-14-40-3D In distribution
NV-8-30-HELIX In distribution
NV-7-30-HELIX In distribution
NV-3-8-HELIX In distribution
PV-2-6-3D In distribution
PV-4-12-3D In distribution
NV-4-10-HELIX In distribution
NV-5-15-HELIX In distribution
PV-20-50-HELIX In distribution
PV-12-40-3D In distribution
PV-5-15-3D In distribution
PV-3-6-3D In distribution
PV-16-40-3D In distribution
PV-18-40-HELIX In distribution
PV-2-2-3D In distribution
NV-6-20-HELIX In distribution
NV-4-8-HELIX In distribution
NV-10-30-HELIX In distribution
NV-3-4-HELIX In distribution
PV-3-8-3D In distribution
PV-12-30-HELIX In distribution
PV-7-30-3D In distribution
PV-18-40-3D In distribution
PV-4-8-3D In distribution
PV-2-4-3D In distribution
NV-10-20-HELIX Withdrawn
NV-5-10-HELIX Withdrawn
NV-8-20-HELIX Withdrawn
NV-6-12-HELIX Withdrawn
NV-9-20-HELIX Withdrawn
NV-7-20-HELIX Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prestige Coil System Balt USA, LLC 339
Axium™ Detachable Coil System Micro Therapeutics, Inc. 279
Optima Coil System Balt USA, LLC 255
AxiumTM Micro Therapeutics, Inc. 255
Avenir Shanghai Wallaby Medical Technologies Co., Inc. 184
MReye Cook Incorporated 167
Axium™ Prime Detachable Coil System Micro Therapeutics, Inc. 162
Nester Cook Incorporated 160
Axium Micro Therapeutics, Inc. 146
ConcertoTM Micro Therapeutics, Inc. 133
Tornado Cook Incorporated 111
V-Trak MicroVention, Inc. 105

Showing 12 of 158. All products under Device, Vascular, For Promoting Embolization

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K090046 2009-02-27
K081465 2008-08-19

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Concerto Detachable Coil System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Covidien 510(k) number 2010-03-01 Not classified Employee error ev3 has initiated a voluntary removal of two lots of Axium Detachable Coil System for product mislabeling as the lots were swapped in production. 14 units 2012-01-31

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P780011 1988-01-29 MINI BALLOON Bd Becton Dickinson Vacutainer Systems Preanalytic

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