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

TARGET DETACHABLE COIL

K Number: K113412 · Decision Dec 13, 2011
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
179
Applicant Total
10
Review Days
25

Basic Information

Device Name
TARGET DETACHABLE COIL
K Number
K113412
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STRYKER NEUROVASCULAR
Date Received
November 18, 2011
Decision Date
December 13, 2011
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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