MOSS VRS Spinal System
K-Number: K181821 · 2018-09-13
Device Summary
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 2018-09-13. The listed applicant is Biedermann Motech GmbH & Co. KG. The 510(k) number is K181821.
When did MOSS VRS Spinal System receive FDA 510(k) clearance?
MOSS VRS Spinal System received FDA 510(k) clearance on 2018-09-13, under 510(k) number K181821.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.