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FDA 510(k) Application Details - K960685
Device Classification Name
Template
More FDA Info for this Device
510(K) Number
K960685
Device Name
Template
Applicant
INTEGRATED SURGICAL SYSTEMS, INC.
829 WEST STADIUM LN.
SACRAMENTO, CA 95834 US
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Contact
ROBERT VAN OSDEL
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Regulation Number
888.4800
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Classification Product Code
HWT
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More FDA Info for this Product Code
Date Received
02/20/1996
Decision Date
01/17/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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