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

MATRIX STRETCH RESISTANT DETACHABLE COIL

K Number: K031168 · Decision May 14, 2003
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
184
Applicant Total
19
Review Days
30

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Basic Information

Device Name
MATRIX STRETCH RESISTANT DETACHABLE COIL
K Number
K031168
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Boston Scientific, Target
Date Received
April 14, 2003
Decision Date
May 14, 2003
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
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K022357 TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 46-815
K021494 GDC POWER SUPPLY, MODEL GDC POWER SUPPLY: 451007-4
K014109 IN-TIME RETRIEVAL DEVICE
K012985 MATRIX DETACHABLE COILS
K013789 EXCELSIOR SL-10 MICROCATHETER, MODELS 168581, 168381, 168181, 168189
K010853 GUIDER SOFTIP GUIDING CATHETER XF 5F
K010707 ATLANTIS SR PLUS CORONARY IMAGING CATHETER, MODEL 35975
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