FDA 510(k), K212747, Da Vinci SP Surgical System
FDA 510(k), K212747, Da Vinci SP Surgical System
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510(K) Number: K212747
Device Name: Da Vinci SP Surgical System
Manufacturer: Connor McCarty
Device Classification Name: System, Surgical, Computer Controlled Instrument
Regulation Number: NAY
Classification Product Code: 08/30/2021
Date Received: 09/29/2021
Decision Date: SE - With Limitations (SESU)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Da Vinci SP Surgical System
Manufacturer: Connor McCarty
Device Classification Name: System, Surgical, Computer Controlled Instrument
Regulation Number: NAY
Classification Product Code: 08/30/2021
Date Received: 09/29/2021
Decision Date: SE - With Limitations (SESU)
Regulation Medical Specialty: General & Plastic Surgery
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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