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FDA 510(k)

Robotic Integration Instruments

K-Number: K233256 · 2024-06-17

ApplicantDePuy Synthes
Decision Date2024-06-17
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Robotic Integration Instruments is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Synthes. It received FDA 510(k) clearance on 2024-06-17 under 510(k) number K233256. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Robotic Integration Instruments?

Robotic Integration Instruments is a medical device that received FDA 510(k) clearance on 2024-06-17. The listed applicant is DePuy Synthes. The 510(k) number is K233256.

When did Robotic Integration Instruments receive FDA 510(k) clearance?

Robotic Integration Instruments received FDA 510(k) clearance on 2024-06-17, under 510(k) number K233256.

Who is the listed applicant for Robotic Integration Instruments?

The FDA 510(k) record lists DePuy Synthes as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Robotic Integration Instruments?

The FDA product code for Robotic Integration Instruments is OLO.

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Related Devices (Code: OLO)

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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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