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FDA 510(k)

da Vinci SP Instruments (SP1098)

K-Number: K241814 · 2024-11-18

ApplicantIntuitive Surgical, Inc.
Decision Date2024-11-18
Product CodeNAY
Advisory CommitteeGU
DecisionUnknown

Device Summary

da Vinci SP Instruments (SP1098) is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2024-11-18 under approval number K241814. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the da Vinci SP Instruments (SP1098)?

da Vinci SP Instruments (SP1098) is a medical device that received FDA 510(k) clearance on 2024-11-18. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K241814.

When was da Vinci SP Instruments (SP1098) approved by the FDA?

da Vinci SP Instruments (SP1098) received FDA 510(k) clearance on 2024-11-18, under approval number K241814.

What company makes da Vinci SP Instruments (SP1098)?

da Vinci SP Instruments (SP1098) is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for da Vinci SP Instruments (SP1098)?

The FDA product code for da Vinci SP Instruments (SP1098) is NAY.

Related Clinical Trials

NCT05672368 The da Vinci Single Port Robotic System for Use in Abdominal and Pelvic Surgical Procedures RECRUITING

Other Devices by Intuitive Surgical, Inc.

K162411da Vinci Xi 12 – 8 mm Reducer K153276da Vinci Xi Surgical System K161271da Vinci Xi Surgical System K152578da Vinci Surgical System, Model IS4000 K152448da Vinci Single-Site Instrument and Accessories K152421IS4000 Stapler 30 Instrument and Stapler 30 Reloads

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Related Devices (Code: NAY)

K162411da Vinci Xi 12 – 8 mm ReducerIntuitive Surgical, Inc. K153276da Vinci Xi Surgical SystemIntuitive Surgical, Inc. K161271da Vinci Xi Surgical SystemIntuitive Surgical, Inc. K152892da Vinci Xi Surgical SystemIntuitive Surgical K152578da Vinci Surgical System, Model IS4000Intuitive Surgical, Inc. K152448da Vinci Single-Site Instrument and AccessoriesIntuitive Surgical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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