FDA 510(k)

Erisma LP Navigated Instruments

K-Number: K202956 · 2021-02-26

Decision Date2021-02-26

Product CodeOLO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Erisma LP Navigated Instruments is a medical device manufactured by Clariance, Sas. It received FDA 510(k) clearance on 2021-02-26 under approval number K202956. 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 Erisma LP Navigated Instruments?

Erisma LP Navigated Instruments is a medical device that received FDA 510(k) clearance on 2021-02-26. It is manufactured by Clariance, Sas. The 510(k) number is K202956.

When was Erisma LP Navigated Instruments approved by the FDA?

Erisma LP Navigated Instruments received FDA 510(k) clearance on 2021-02-26, under approval number K202956.

What company makes Erisma LP Navigated Instruments?

Erisma LP Navigated Instruments is manufactured by Clariance, Sas.

What is the FDA product code for Erisma LP Navigated Instruments?

The FDA product code for Erisma LP Navigated 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.