NanoBone® SBX Putty ; NanoBone® QD
K-Number: K250521 · 2025-04-07
ApplicantBiocomposites, Ltd.
Decision Date2025-04-07
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NanoBone® SBX Putty ; NanoBone® QD is a medical device manufactured by Biocomposites, Ltd.. It received FDA 510(k) clearance on 2025-04-07 under approval number K250521. 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 NanoBone® SBX Putty ; NanoBone® QD?
NanoBone® SBX Putty ; NanoBone® QD is a medical device that received FDA 510(k) clearance on 2025-04-07. It is manufactured by Biocomposites, Ltd.. The 510(k) number is K250521.
When was NanoBone® SBX Putty ; NanoBone® QD approved by the FDA?
NanoBone® SBX Putty ; NanoBone® QD received FDA 510(k) clearance on 2025-04-07, under approval number K250521.
What company makes NanoBone® SBX Putty ; NanoBone® QD?
NanoBone® SBX Putty ; NanoBone® QD is manufactured by Biocomposites, Ltd..
What is the FDA product code for NanoBone® SBX Putty ; NanoBone® QD?
The FDA product code for NanoBone® SBX Putty ; NanoBone® QD is MQV.
Other Devices by Biocomposites, Ltd.
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.