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FDA 510(k)

VIPER PRIME™ Screws with Fenestrations

K-Number: K170543 · 2017-05-04

ApplicantMedos International SARL
Decision Date2017-05-04
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VIPER PRIME™ Screws with Fenestrations is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2017-05-04 under approval number K170543. 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 VIPER PRIME™ Screws with Fenestrations?

VIPER PRIME™ Screws with Fenestrations is a medical device that received FDA 510(k) clearance on 2017-05-04. It is manufactured by Medos International SARL. The 510(k) number is K170543.

When was VIPER PRIME™ Screws with Fenestrations approved by the FDA?

VIPER PRIME™ Screws with Fenestrations received FDA 510(k) clearance on 2017-05-04, under approval number K170543.

What company makes VIPER PRIME™ Screws with Fenestrations?

VIPER PRIME™ Screws with Fenestrations is manufactured by Medos International SARL.

What is the FDA product code for VIPER PRIME™ Screws with Fenestrations?

The FDA product code for VIPER PRIME™ Screws with Fenestrations is NKB.

Other Devices by Medos International SARL

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Related Devices (Code: NKB)

K163301CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc. K162134ENNOVATE Spinal SystemAesculap Implant Systems, LLC K162912VIPER PRIME™ additions to the VIPER® SystemMedos International SARL K162160Preference Elite Pedicle Screw SystemAmedica Corporation K162232MOSS 100 Pedicle Screw SystemBiedermann Motech GmbH & Co. KG K162379CD HORIZON® Spinal SystemMedtronic Sofamor Danek USA, Inc.

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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