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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 a medical device manufactured by DePuy Synthes. It received FDA 510(k) clearance on 2024-06-17 under approval 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. It is manufactured by DePuy Synthes. The 510(k) number is K233256.

When was Robotic Integration Instruments approved by the FDA?

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

What company makes Robotic Integration Instruments?

Robotic Integration Instruments is manufactured by DePuy Synthes.

What is the FDA product code for Robotic Integration Instruments?

The FDA product code for Robotic Integration Instruments is OLO.

Related Clinical Trials

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Related PubMed Literature

PMID: 42174947 Aligning AI-Native 6G Healthcare Systems with EU Ethical and Legal Frameworks. Studies in health technology and informatics (2026) PMID: 41725549 Ethical and legal challenges of integrating artificial intelligence into paediatric surgery. Annals of the Royal College of Surgeons of England (2026) PMID: 41619565 Integration of materiovigilance in Unani medicine: A step towards patient safety. Journal of Ayurveda and integrative medicine (2026) PMID: 41513582 Medical devices for professional use: What assessment, what funding? Therapie (2026)

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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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