Uni-FuZe-P Bone Putty
K-Number: K201781 · 2020-12-28
ApplicantZavation Medical Products, LLC
Decision Date2020-12-28
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Uni-FuZe-P Bone Putty is a medical device manufactured by Zavation Medical Products, LLC. It received FDA 510(k) clearance on 2020-12-28 under approval number K201781. 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-P Bone Putty?
Uni-FuZe-P Bone Putty is a medical device that received FDA 510(k) clearance on 2020-12-28. It is manufactured by Zavation Medical Products, LLC. The 510(k) number is K201781.
When was Uni-FuZe-P Bone Putty approved by the FDA?
Uni-FuZe-P Bone Putty received FDA 510(k) clearance on 2020-12-28, under approval number K201781.
What company makes Uni-FuZe-P Bone Putty?
Uni-FuZe-P Bone Putty is manufactured by Zavation Medical Products, LLC.
What is the FDA product code for Uni-FuZe-P Bone Putty?
The FDA product code for Uni-FuZe-P Bone Putty is MQV.
Other Devices by Zavation Medical Products, LLC
Related Devices (Code: MQV)
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.