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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
FDA Hosted 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
FDA Hosted 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