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

THROMCAT THROMBECTOMY CATHETER SYSTEM

K Number: K060016 · Decision Apr 25, 2006
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
145
Applicant Total
19
Review Days
112

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Basic Information

Device Name
THROMCAT THROMBECTOMY CATHETER SYSTEM
K Number
K060016
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kensey Nash Corp.
Date Received
January 3, 2006
Decision Date
April 25, 2006
Product Code
MCW
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
MCW Catheter, Peripheral, Atherectomy

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K Number Device Name
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K090919 KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANE
K073519 QUICKCAT EXTRACTION CATHETER, MODEL 60090-01
K071695 KENSEY NASH MACROPORE SHIELD
K072384 MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE
K072195 THROMCAT THROMBECTOMY CATHETER SYSTEM
K071237 COPIOS BONE VOID FILLER SPONGE AND PASTE
K062870 TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03
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