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

WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM

K Number: K000001 · Decision Jun 5, 2000
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
44
Applicant Total
35
Review Days
154

Basic Information

Device Name
WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM
K Number
K000001
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
BOSTON SCIENTIFIC SCIMED, INC.
Date Received
January 3, 2000
Decision Date
June 5, 2000
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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K021901 WALLGRAFT TRACHEOBRONCHIAL ENDOPROTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
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K012216 NIROYAL BILIARY PREMOUNTED STENT SYSTEM
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