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MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS P4028/FG08300

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061063
510(k) Type
Special
Applicant
Foxhollow Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2006
Days to Decision
31 days
Submission Type
Summary

MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS P4028/FG08300

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061063
510(k) Type
Special
Applicant
Foxhollow Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2006
Days to Decision
31 days
Submission Type
Summary