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FDA 510(k)

VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS

K-Number: K120867 · 2012-09-20

ApplicantMedos International SARL
Decision Date2012-09-20
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2012-09-20 under 510(k) number K120867. 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 VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS?

VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2012-09-20. The listed applicant is Medos International SARL. The 510(k) number is K120867.

When did VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS receive FDA 510(k) clearance?

VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS received FDA 510(k) clearance on 2012-09-20, under 510(k) number K120867.

Who is the listed applicant for VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS?

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

What is the FDA product code for VIPER AND EXPEDIUM NAVIGATED INSTRUMENTS?

The FDA product code for VIPER AND EXPEDIUM NAVIGATED 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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