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FDA 510(k)

Additional VIPER PRIME™ screws with fenestrations

K-Number: K171570 · 2017-08-31

ApplicantMedos International SARL
Decision Date2017-08-31
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Additional VIPER PRIME™ screws with fenestrations 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 2017-08-31 under 510(k) number K171570. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Additional VIPER PRIME™ screws with fenestrations?

Additional VIPER PRIME™ screws with fenestrations is a medical device that received FDA 510(k) clearance on 2017-08-31. The listed applicant is Medos International SARL. The 510(k) number is K171570.

When did Additional VIPER PRIME™ screws with fenestrations receive FDA 510(k) clearance?

Additional VIPER PRIME™ screws with fenestrations received FDA 510(k) clearance on 2017-08-31, under 510(k) number K171570.

Who is the listed applicant for Additional VIPER PRIME™ screws with fenestrations?

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 Additional VIPER PRIME™ screws with fenestrations?

The FDA product code for Additional VIPER PRIME™ screws with fenestrations is NKB.

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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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