Medical Device Manufacturer · US , Sunnyvale , CA

Medtronic Percusurge, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Recent clearances: PERCUSURGE GUARDWIRE PLUS TEMPORARY OCCLUSION AND ASPIRATION SYSTEM, MODIFICATION TO GUARDWIRE PLUS TEMPORARY OCCLUSION & ASPIRATION SYSTEM

View 2 510(k) Devices ↓
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Medtronic Percusurge, Inc. Cardiovascular ✕

2 devices
1-2 of 2
Cleared Nov 15, 2002
PERCUSURGE GUARDWIRE PLUS TEMPORARY OCCLUSION AND ASPIRATION SYSTEM
K013913 · NFA
Cardiovascular · 353d
Cleared Jan 25, 2002
MODIFICATION TO GUARDWIRE PLUS TEMPORARY OCCLUSION & ASPIRATION SYSTEM
K014223 · NFA
Cardiovascular · 30d
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