FDA 510(k) Application Details - K251213

Device Classification Name System,Surgical,Computer Controlled Instrument

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510(K) Number K251213
Device Name System,Surgical,Computer Controlled Instrument
Applicant Intuitive Surgical, Inc.
1266 Kifer Road
Sunnyvale, CA 94086 US
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Contact Jennifer Karafin
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Regulation Number 876.1500

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Classification Product Code NAY
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Date Received 04/18/2025
Decision Date 07/23/2025
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K251213


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