FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Penumbra Smart Coil

K Number: K143218 · Decision Mar 18, 2015
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
184
Applicant Total
87
Review Days
128

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Basic Information

Device Name
Penumbra Smart Coil
K Number
K143218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Penumbra, Inc.
Date Received
November 10, 2014
Decision Date
March 18, 2015
Product Code
HCG
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HCG Device, Neurovascular Embolization

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Other Clearances by Penumbra, Inc.

K Number Device Name
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K252612 INDIGO® Aspiration System – Lightning Flash Aspiration Tubing; INDIGO® Aspiration System – Lightning Bolt Aspiration Tubing
K250079 Ruby XL System
K242104 Penumbra System (Reperfusion Catheter RED 72)
K242033 Access25™ Delivery Microcatheter
K242520 Element Vascular Access System
K242075 Indigo® Aspiration System – Lightning Bolt Aspiration Tubing
K242319 Indigo® Aspiration System – Aspiration Catheter 6X
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