Wallgraft Tracheobronchial Endoprothesis with Unistep Plus Delivery System

FDA 510(k) K021901 · Boston Scientific Scimed, Inc.

Substantially Equivalent

510(k) numberK021901

Submission

Device name
Wallgraft Tracheobronchial Endoprothesis with Unistep Plus Delivery System
Applicant
Boston Scientific Scimed, Inc.
Maple Grove, MN, US
Received
June 10, 2002
Decision date
July 9, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JCT – Prosthesis, Tracheal, Expandable
Device class
Class II (moderate risk)
Regulation
21 CFR 878.3720
Specialty
General, Plastic Surgery
Implant
Yes
Life-sustaining
Yes

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More from Boston Scientific Corporation

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K041727Modification to Atlantis PV Imaging Catheter, Model 36456OBJ · Special 07/23/2004SE
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K024048Modification to Boston Scientific Express Biliary LD Premounted Stent SystemFGE · Special 01/06/2003SESU
K021735Boston Scientific Ultra-Soft SV Balloon Dilatation CatheterDQY · Traditional 08/08/2002SE
K012822Modificiation to: Biliary Wallstent Endoprostheis with Monorail Delivery System, Model…FGE · Special 10/24/2001SESU
K012216Niroyal Biliary Premounted Stent SystemFGE · Special 08/17/2001SESU
K000743Boston Scientific Scimed Atlantis Coronary Imaging Catheter, Model C4020DQO · Traditional 09/06/2000SE
K000001Wallgraft Tracheobronchial Endoprosthesis and Unistep Delivery SystemJCT · Traditional 06/05/2000SE
K000956Modification to Scimed 6F Impulse Angiographic CathatersDQO · Special 04/21/2000SE
K993232Wallstent Biliary Endoprosthesis and Unistep Plus Delivery SystemFGE · Traditional 12/30/1999SESU

Questions and answers

When was Wallgraft Tracheobronchial Endoprothesis with Unistep Plus Delivery System cleared by the FDA?

Wallgraft Tracheobronchial Endoprothesis with Unistep Plus Delivery System (K021901) received a 510(k) decision of Substantially Equivalent on July 9, 2002, 29 days after the submission was received.

What is the product code of K021901?

The FDA product code is JCT – Prosthesis, Tracheal, Expandable, a Class II (moderate risk) device regulated under 21 CFR 878.3720.