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

AXIUM DETACHABLE COIL SYSTEM

K Number: K081465 · Decision Aug 19, 2008
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
128
Applicant Total
51
Review Days
84

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Basic Information

Device Name
AXIUM DETACHABLE COIL SYSTEM
K Number
K081465
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micro Therapeutics, Inc.
Date Received
May 27, 2008
Decision Date
August 19, 2008
Product Code
KRD
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
KRD Device, Vascular, For Promoting Embolization

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Other Clearances by Micro Therapeutics, Inc.

K Number Device Name
K113289 ORION MICRO CATHETER
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K090870 ECHELON MICRO CATHETER, MODELS 105-5092-150SA, 145-5092-150SA AND 190-5092-150SA AND SYRINGE ADAPTER ACCESSORY
K090046 CONCERTO DETACHABLE COIL SYSTEM
K060747 FX DETACHABLE COIL SYSTEM
K060625 NEXUS DETACHABLE COIL SYSTEM, MORPHEUS 3D CSR
K051990 ECHELON MICRO CATHETER
K051560 NEXUS DETACHABLE COIL, MULTI-DIAMETER CSR AND HELIX SUPER SOFT CSR
K051425 NEXUS DETACHABLE COIL SYSTEM, HELIX SUPER SOFT CSR
K050543 NEXUS DETACHABLE COIL SYSTEM
Search all 51 clearances from Micro Therapeutics, Inc. →