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

STRYKER NAVIGATION SYSTEM-KNEE MODULE

K Number: K010204 · Decision Aug 31, 2001
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
124
Review Days
220

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Basic Information

Device Name
STRYKER NAVIGATION SYSTEM-KNEE MODULE
K Number
K010204
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corp.
Date Received
January 23, 2001
Decision Date
August 31, 2001
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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