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

STRYKER KWIC NEEDLE

K Number: K140868 · Decision Jun 5, 2014
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
23
Review Days
63

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Basic Information

Device Name
STRYKER KWIC NEEDLE
K Number
K140868
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthovita, Inc.
Date Received
April 3, 2014
Decision Date
June 5, 2014
Product Code
HAW
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
HAW Neurological Stereotaxic Instrument

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K091618 VITOMATRIX
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