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 a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2017-08-31 under approval 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. It is manufactured by Medos International SARL. The 510(k) number is K171570.
When was Additional VIPER PRIME screws with fenestrations approved by the FDA?
Additional VIPER PRIME screws with fenestrations received FDA 510(k) clearance on 2017-08-31, under approval number K171570.
What company makes Additional VIPER PRIME screws with fenestrations?
Additional VIPER PRIME screws with fenestrations is manufactured by Medos International SARL.
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.