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FDA 510(k)

CROSSNAV Navigation Enabled Instruments

K-Number: K233255 · 2024-06-17

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

Device Summary

CROSSNAV Navigation Enabled Instruments is a medical device manufactured by DePuy Synthes. It received FDA 510(k) clearance on 2024-06-17 under approval number K233255. 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 CROSSNAV Navigation Enabled Instruments?

CROSSNAV Navigation Enabled 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 K233255.

When was CROSSNAV Navigation Enabled Instruments approved by the FDA?

CROSSNAV Navigation Enabled Instruments received FDA 510(k) clearance on 2024-06-17, under approval number K233255.

What company makes CROSSNAV Navigation Enabled Instruments?

CROSSNAV Navigation Enabled Instruments is manufactured by DePuy Synthes.

What is the FDA product code for CROSSNAV Navigation Enabled Instruments?

The FDA product code for CROSSNAV Navigation Enabled Instruments is 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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