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

BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS

K Number: K060121 · Decision Mar 21, 2006
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
93
Review Days
63

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Basic Information

Device Name
BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS
K Number
K060121
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing Corp
Date Received
January 17, 2006
Decision Date
March 21, 2006
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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