510(k) K051621

ENDOVENTIONS ALIMAXX-E ESOPHAGEAL STENT SYSTEM by Alveolus, Inc. — Product Code ESW

K051621 is an FDA 510(k) premarket notification submitted by Alveolus, Inc. for the device "ENDOVENTIONS ALIMAXX-E ESOPHAGEAL STENT SYSTEM". The FDA issued a decision of Substantially Equivalent on July 11, 2005. The device falls under product code ESW (Prosthesis, Esophageal), a Class II device regulated under 21 CFR 878.3610. Alveolus, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 11, 2005
Date Received
June 20, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Esophageal
Device Class
Class II
Regulation Number
878.3610
Review Panel
GU
Submission Type