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FDA 510(k)

MOSS VRS Spinal System

K-Number: K203607 · 2021-08-20

ApplicantBiedermann Motech GmbH & Co. KG
Decision Date2021-08-20
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOSS VRS Spinal System is a medical device manufactured by Biedermann Motech GmbH & Co. KG. It received FDA 510(k) clearance on 2021-08-20 under approval number K203607. 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 MOSS VRS Spinal System?

MOSS VRS Spinal System is a medical device that received FDA 510(k) clearance on 2021-08-20. It is manufactured by Biedermann Motech GmbH & Co. KG. The 510(k) number is K203607.

When was MOSS VRS Spinal System approved by the FDA?

MOSS VRS Spinal System received FDA 510(k) clearance on 2021-08-20, under approval number K203607.

What company makes MOSS VRS Spinal System?

MOSS VRS Spinal System is manufactured by Biedermann Motech GmbH & Co. KG.

What is the FDA product code for MOSS VRS Spinal System?

The FDA product code for MOSS VRS Spinal System is NKB.

Related Clinical Trials

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Related PubMed Literature

PMID: 41612341 Brain-computer interface commercialization. Journal of neuroengineering and rehabilitation (2026) PMID: 39726899 How to improve the mechanical safety of a novel spinal implant while saving costs and time. JOR spine (2024)

Other Devices by Biedermann Motech GmbH & Co. KG

K162232MOSS 100 Pedicle Screw System K170890TELIX K Interbody System K181821MOSS VRS Spinal System

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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