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

Excelsior XT-17 Microcatheter, Excelsior XT-17 Flex Microcatheter, Excelsior XT-17 Pre-Shaped Microcatheter, Excelsior XT-17 Flex Pre-Shaped Microcatheter

K Number: K142565 · Decision Nov 14, 2014
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
32
Review Days
63

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Basic Information

Device Name
Excelsior XT-17 Microcatheter, Excelsior XT-17 Flex Microcatheter, Excelsior XT-17 Pre-Shaped Microcatheter, Excelsior XT-17 Flex Pre-Shaped Microcatheter
K Number
K142565
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Neurovascular
Date Received
September 12, 2014
Decision Date
November 14, 2014
Product Code
DQY
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
DQY Catheter, Percutaneous

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