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

VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER)

K Number: K071962 · Decision Sep 26, 2007
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
184
Applicant Total
37
Review Days
72

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Basic Information

Device Name
VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER)
K Number
K071962
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5950
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cordis Neurovascular, Inc.
Date Received
July 16, 2007
Decision Date
September 26, 2007
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HCG), ordered by most recent decision date.

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Other Clearances by Cordis Neurovascular, Inc.

K Number Device Name
K082324 TRUFILL DCS SYRINGE
K080967 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE OR TRUFILL DCS SYRINGE II, ALSO KNOWN AS THE TRUFILL DCS ORBIT
K070279 MODIFICATION TO HYPERTRANSIT INFUSION CATHETER
K063254 THE TRUFILL DCS DETACHABLE COIL SYSTEM; THE TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM
K053197 TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM LINE EXTENSION
K043538 HYPERTRANSIT INFUSION CATHETER
K032553 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM
K030963 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS THE TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM
K021591 PROWLER SELECT (10, 14, AND PLUS) INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
K020680 PROWLER SELECT 10 AND 14 INFUSION CATHETERS WITH AND WITHOUT PRE-SHAPED TIPS
Search all 37 clearances from Cordis Neurovascular, Inc. →