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SMITHWICK CAROTID SHUNT

Page Type
Cleared 510(K)
510(k) Number
K021608
510(k) Type
Traditional
Applicant
IMPLANTABLE DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2002
Days to Decision
159 days
Submission Type
Statement

SMITHWICK CAROTID SHUNT

Page Type
Cleared 510(K)
510(k) Number
K021608
510(k) Type
Traditional
Applicant
IMPLANTABLE DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2002
Days to Decision
159 days
Submission Type
Statement