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FDA 510(k), K171699, da Vinci Xi Surgical System, da Vinci Si Surgical System, da Vinci X Surgical System
FDA 510(k), K171699, da Vinci Xi Surgical System, da Vinci Si Surgical System, da Vinci X Surgical System
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510(K) Number: K171699
Device Name: da Vinci Xi Surgical System, da Vinci Si Surgical System, da Vinci X Surgical System
Manufacturer: Brandon Hansen
Device Classification Name: System, Surgical, Computer Controlled Instrument
Regulation Number: NAY
Classification Product Code: KXA
Date Received: 06/08/2017
Decision Date: 07/28/2017
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: da Vinci Xi Surgical System, da Vinci Si Surgical System, da Vinci X Surgical System
Manufacturer: Brandon Hansen
Device Classification Name: System, Surgical, Computer Controlled Instrument
Regulation Number: NAY
Classification Product Code: KXA
Date Received: 06/08/2017
Decision Date: 07/28/2017
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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