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FDA 510(k) Application Details - K962792
Device Classification Name
Accelerator, Linear, Medical
More FDA Info for this Device
510(K) Number
K962792
Device Name
Accelerator, Linear, Medical
Applicant
SURGICAL NAVIGATION TECHNOLOGIES, INC.
530 COMPTON ST.
BROOMFIELD, CO 80020 US
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Contact
KURT R SMITH
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Regulation Number
892.5050
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Classification Product Code
IYE
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More FDA Info for this Product Code
Date Received
07/17/1996
Decision Date
11/12/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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