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FDA 510(k)

MOSS VRS Spinal System

K-Number: K203607 · 2021-08-20

Decision Date2021-08-20
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOSS VRS Spinal System is the device name listed in this FDA 510(k) record. The listed applicant is Biedermann Motech GmbH & Co. KG. It received FDA 510(k) clearance on 2021-08-20 under 510(k) 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. The listed applicant is Biedermann Motech GmbH & Co. KG. The 510(k) number is K203607.

When did MOSS VRS Spinal System receive FDA 510(k) clearance?

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

Who is the listed applicant for MOSS VRS Spinal System?

The FDA 510(k) record lists Biedermann Motech GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Biedermann Motech GmbH & Co. KG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NKB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.