Savvy

PTA Savvy Small Vessel 3.5X10

Registry build 21.09.26
5manufacturers in China registered for this device type
85catalogue numbers in this listing
30510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (3), Guangdong (2).

Chinese manufacturers registered for FDA product code LIT
Manufacturer City Province Registered as Device types
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Savvy
Listed by Cordis Corp., United States
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
Record published 2016-08-01
Record revised 2023-10-12 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Store in cool, dark, dry place; Special storage condition: Do not use if package is damanged
Distribution end date 2019-09-30

Catalogue Numbers

Catalogue numbers for Savvy
Catalogue number Size Status
435354X Withdrawn
435504L Withdrawn
435204L Withdrawn
435200S Withdrawn
435350L Withdrawn
435250L Withdrawn
435604L Withdrawn
435506S Withdrawn
435456S Withdrawn
435602L Withdrawn
435506L Withdrawn
435456L Withdrawn
435403L Withdrawn
435254L Withdrawn
435304X Withdrawn
435302S Withdrawn
435253L Withdrawn
435600L Withdrawn
435254S Withdrawn
435400L Withdrawn
435203L Withdrawn
435352L Withdrawn
435300X Withdrawn
435454L Withdrawn
435556L Withdrawn
435306L Withdrawn
435250S Withdrawn
435552S Withdrawn
435354L Withdrawn
435504S Withdrawn
435606S Withdrawn
435300S Withdrawn
435600S Withdrawn
435256S Withdrawn
435304S Withdrawn
435200L Withdrawn
435302X Withdrawn
435252S Withdrawn
435256L Withdrawn
435254X Withdrawn
435404S Withdrawn
435500L Withdrawn
435356S Withdrawn
435200X Withdrawn
435300L Withdrawn
435354S Withdrawn
435302L Withdrawn
435452S Withdrawn
435402S Withdrawn
435350S Withdrawn
435554S Withdrawn
435502L Withdrawn
435353L Withdrawn
435303L Withdrawn
435400S Withdrawn
435352X Withdrawn
435304L Withdrawn
435202S Withdrawn
435204X Withdrawn
435452L Withdrawn
435252X Withdrawn
435454S Withdrawn
435502S Withdrawn
435406S Withdrawn
435206L Withdrawn
435500S Withdrawn
435206S Withdrawn
435352S Withdrawn
435406L Withdrawn
435402L Withdrawn
435402X Withdrawn
435204S Withdrawn
435356L Withdrawn
435404L Withdrawn
435202X Withdrawn
435306S Withdrawn
435552L Withdrawn
435606L Withdrawn
435604S Withdrawn
435252L Withdrawn
435404X Withdrawn
435400X Withdrawn
435602S Withdrawn
435202L Withdrawn
435554L Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Parafleet SC 018 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 1,460
Jade Plus PTA Balloon Dilatation Catheter / Jade Plus 18 OTW OrbusNeich Medical (Shenzhen) Co., Ltd. 832
Jade PTA Balloon Dilatation Catheter OrbusNeich Medical (Shenzhen) Co., Ltd. 667
Parafleet SC 014 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 572
Minerva PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 504
Advocate Arravasc, Ltd. 441
Ultraverse® 035 PTA Dilatation Catheter Bard Peripheral Vascular, Inc. 361
Polux PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 359
Advance Cook Incorporated 355
Pacific™ Plus Medtronic, Inc. 347
EverCross™ ev3, Inc. 316
Achilles NC PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 297

Showing 12 of 167. All products under Catheter, Angioplasty, Peripheral, Transluminal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K210626 2021-04-23
K201377 2020-10-09
K201333 2020-09-11
K133843 2014-06-27
K121442 2012-06-14
K112797 2012-05-04
K050645 2005-04-01
K003159 2000-10-30
K992825 1999-09-15
K991811 1999-06-15
K981407 1998-05-20
K971516 1997-07-23
K971579 1997-07-18
K971448 1997-07-03
K971010 1997-06-18
K970620 1997-05-06
K970299 1997-04-24
K963000 1997-02-20
K962945 1996-10-23
K955886 1996-03-11
K950119 1995-05-17
K946052 1995-03-03
K942094 1994-11-01
K940868 1994-07-12
K933236 1993-12-27
K905698 1991-07-09
K894899 1990-01-26
K880612 1988-07-28
K844913 1985-08-20
K812168 1981-08-31

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