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Foxhollow Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K061188 SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEMMCW2006-10-23 View
510(k) K061063 MODIFICATION TO: SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS P4028/FG08300MCW2006-05-18 View
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