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

POD SYSTEM

K Number: K141134 · Decision Jul 3, 2014
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
179
Applicant Total
31
Review Days
63

Basic Information

Device Name
POD SYSTEM
K Number
K141134
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PENUMBRA, INC.
Date Received
May 1, 2014
Decision Date
July 3, 2014
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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K Number Device Name
K163618 INDIGO Aspiration System
K160449 Penumbra System, Penumbra Pump MAX
K160533 Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)
K160832 Penumbra Smart Coil
K152699 Apollo System
K152541 Penumbra System ACE 64 and ACE 68 Reperfusion Catheters
K152840 Lantern Delivery Microcatheter
K151572 Penumbra Smart Coil
K142870 Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]
K142458 Penumbra System ACE
Search all 31 clearances from PENUMBRA, INC. →