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MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300,

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053460
510(k) Type
Special
Applicant
Fox Hollow Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2006
Days to Decision
31 days
Submission Type
Summary

MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300,

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053460
510(k) Type
Special
Applicant
Fox Hollow Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2006
Days to Decision
31 days
Submission Type
Summary