Sterling Over-The-Wire (Otw) Pta Balloon Dilatation Catheter

FDA 510(k) K132430 · Boston Scientific Corp

Substantially Equivalent

510(k) numberK132430

Submission

Device name
Sterling Over-The-Wire (Otw) Pta Balloon Dilatation Catheter
Applicant
Boston Scientific Corp
Maple Grove, MN, US
Received
August 5, 2013
Decision date
October 17, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LIT – Catheter, Angioplasty, Peripheral, Transluminal
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1250
Specialty
Cardiovascular

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K260304WAVE PTA Balloon CatheterLIT · Traditional WAVE Medical AG05/20/2026SE
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K251915Amethyst HP PTA OTW 0.035 CatheterLIT · Traditional Natec Medical , Ltd.12/18/2025SE
K250706Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters…LIT · Special Biotronik, Inc.04/04/2025SE
K243704Parafleet SC 014 PTA Balloon Dilatation Catheter; Parafleet SC 018 PTA Balloon…LIT · Traditional Brosmed Medical Co., Ltd.02/27/2025SE
K241040Amethyst HP PTA OTW 0.035 CatheterLIT · Traditional Natec Medical , Ltd.12/18/2024SE
K242419018 Hydrophilic Coated OTW PTA Balloon Dilatation CatheterLIT · Traditional Creagh Medical Ltd. Dba Surmodics, Inc.11/15/2024SE
K241740Finesse Injectable™ PTA Balloon Dilatation CatheterLIT · Special Summa Therapeutics07/16/2024SE
K241711Oscar Peripheral Multifunctional Catheter systemLIT · Special Biotronik, Inc.07/11/2024SE
K241683Sterling™ MONORAIL™ PTA Balloon Dilatation Catheter (H74939031404020 ); Sterling™…LIT · Special Boston Scientific Corporation07/10/2024SE

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Questions and answers

When was Sterling Over-The-Wire (Otw) Pta Balloon Dilatation Catheter cleared by the FDA?

Sterling Over-The-Wire (Otw) Pta Balloon Dilatation Catheter (K132430) received a 510(k) decision of Substantially Equivalent on October 17, 2013, 73 days after the submission was received.

What is the product code of K132430?

The FDA product code is LIT – Catheter, Angioplasty, Peripheral, Transluminal, a Class II (moderate risk) device regulated under 21 CFR 870.1250.