510(k) K071604

ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEM by Alveolus, Inc. — Product Code JCT

K071604 is an FDA 510(k) premarket notification submitted by Alveolus, Inc. for the device "ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEM". The FDA issued a decision of SESU on September 19, 2007. The device falls under product code JCT (Prosthesis, Tracheal, Expandable), a Class II device regulated under 21 CFR 878.3720. Alveolus, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESU ()
Decision Date
September 19, 2007
Date Received
June 12, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Tracheal, Expandable
Device Class
Class II
Regulation Number
878.3720
Review Panel
AN
Submission Type