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SMITHWICK CAROTID SHUNT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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