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FDA 510(k)

Uni-FuZe-C Bone Strip

K-Number: K221726 · 2023-01-18

Decision Date2023-01-18
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Uni-FuZe-C Bone Strip is the device name listed in this FDA 510(k) record. The listed applicant is Zavation Medical Products, LLC. It received FDA 510(k) clearance on 2023-01-18 under 510(k) number K221726. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Uni-FuZe-C Bone Strip?

Uni-FuZe-C Bone Strip is a medical device that received FDA 510(k) clearance on 2023-01-18. The listed applicant is Zavation Medical Products, LLC. The 510(k) number is K221726.

When did Uni-FuZe-C Bone Strip receive FDA 510(k) clearance?

Uni-FuZe-C Bone Strip received FDA 510(k) clearance on 2023-01-18, under 510(k) number K221726.

Who is the listed applicant for Uni-FuZe-C Bone Strip?

The FDA 510(k) record lists Zavation Medical Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Uni-FuZe-C Bone Strip?

The FDA product code for Uni-FuZe-C Bone Strip is MQV.

Other records listing Zavation Medical Products, LLC 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.

View all 31 devices →

Related Devices (Code: MQV)

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.