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FDA 510(k)

Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set

K-Number: K212756 · 2022-05-05

ApplicantMedos International SARL
Decision Date2022-05-05
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2022-05-05 under approval number K212756. 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 Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set?

Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set is a medical device that received FDA 510(k) clearance on 2022-05-05. It is manufactured by Medos International SARL. The 510(k) number is K212756.

When was Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set approved by the FDA?

Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set received FDA 510(k) clearance on 2022-05-05, under approval number K212756.

What company makes Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set?

Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set is manufactured by Medos International SARL.

What is the FDA product code for Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set?

The FDA product code for Discectomy Navigation Ready Instruments and Universal Navigation Adaptor Set 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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