FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ALVEOLUS, TB-STS TRACHEOBRONCHIAL STENT SYSTEM

K Number: K033053 · Decision Feb 25, 2004
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
44
Applicant Total
12
Review Days
149

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Basic Information

Device Name
ALVEOLUS, TB-STS TRACHEOBRONCHIAL STENT SYSTEM
K Number
K033053
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3720
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alveolus, Inc.
Date Received
September 29, 2003
Decision Date
February 25, 2004
Product Code
JCT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JCT Prosthesis, Tracheal, Expandable

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Other Clearances by Alveolus, Inc.

K Number Device Name
K083625 AERO DV TRACHEOBRONCHIAL STENT SYSTEM
K082284 AERO TRACHEOBRONCHIAL STENT TECHNOLOGY SYSTEM
K080838 ALVEOLUS ALIMAXX-E ESOPHAGEAL STENT SYSTEM
K072720 ALIMAXX-B UNCOVERED BILIARY STENT SYSTEM
K071604 ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEM
K062511 AERO TRACHEOBRONCHIAL STENT SYSTEM, MODEL 90129-2XX
K060239 ALEOLUS/ENOVENTIONS,ALIMAXX-E DV ESOPHAGEAL STENT SYSTEM
K051621 ENDOVENTIONS ALIMAXX-E ESOPHAGEAL STENT SYSTEM
K033990 ALVEOLUS INC. TB-STS TRACHEOBRONCHIAL STENT SYSTEM
K032744 ALVEOLUS INC., TB-STS TRACHEOBRONCHIAL STENT SYSTEM
Search all 12 clearances from Alveolus, Inc. →