510(k) K062511
K062511 is an FDA 510(k) premarket notification submitted by Alveolus, Inc. for the device "AERO TRACHEOBRONCHIAL STENT SYSTEM, MODEL 90129-2XX". The FDA issued a decision of SESU on January 31, 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
- January 31, 2007
- Date Received
- August 28, 2006
- 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