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

TRAC-WRIGHT TRAC 10 CATHETER

K Number: K915238 · Decision Feb 19, 1992
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
145
Applicant Total
74
Review Days
90

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Basic Information

Device Name
TRAC-WRIGHT TRAC 10 CATHETER
K Number
K915238
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dow Corning Wright
Date Received
November 21, 1991
Decision Date
February 19, 1992
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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K930189 ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP
K930188 ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT
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