510(k) K083625
K083625 is an FDA 510(k) premarket notification submitted by Alveolus, Inc. for the device "AERO DV TRACHEOBRONCHIAL STENT SYSTEM". The FDA issued a decision of SESU on March 11, 2009. 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
- March 11, 2009
- Date Received
- December 8, 2008
- 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