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FDA 510(k)

Small VBR™

K-Number: K192117 · 2019-11-01

ApplicantUlrich GmbH & Co. KG
Decision Date2019-11-01
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Small VBR™ is the device name listed in this FDA 510(k) record. The listed applicant is Ulrich GmbH & Co. KG. It received FDA 510(k) clearance on 2019-11-01 under 510(k) number K192117. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Small VBR™?

Small VBR™ is a medical device that received FDA 510(k) clearance on 2019-11-01. The listed applicant is Ulrich GmbH & Co. KG. The 510(k) number is K192117.

When did Small VBR™ receive FDA 510(k) clearance?

Small VBR™ received FDA 510(k) clearance on 2019-11-01, under 510(k) number K192117.

Who is the listed applicant for Small VBR™?

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

What is the FDA product code for Small VBR™?

The FDA product code for Small VBR™ is MQP.

Other records listing Ulrich GmbH & Co. KG as applicant

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Related Devices (Code: MQP)

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.

K261810Vertiwedge® Intraosseous SystemFoundation Surgical GroupK261031POSEIDON STSignus Medinzintechnik GmbHK253158VyBrate™ VBR SystemVy Spine, LLCK241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc.K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AGK233359DOMINION Expandable Corpectomy SystemAstura Medical

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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