FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEM

K Number: K071604 · Decision Sep 19, 2007
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
44
Applicant Total
12
Review Days
99

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Basic Information

Device Name
ALVEOLUS AERO DV TRACHEOBRONCHIAL STENT SYSTEM
K Number
K071604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3720
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Summary
Applicant
Alveolus, Inc.
Date Received
June 12, 2007
Decision Date
September 19, 2007
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JCT), ordered by most recent decision date.

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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
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
K033053 ALVEOLUS, TB-STS TRACHEOBRONCHIAL STENT SYSTEM
K032744 ALVEOLUS INC., TB-STS TRACHEOBRONCHIAL STENT SYSTEM
Search all 12 clearances from Alveolus, Inc. →