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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Biocomposites, Ltd.. It received FDA 510(k) clearance on 2025-04-07 under 510(k) 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. The listed applicant is Biocomposites, Ltd.. The 510(k) number is K250521.

When did NanoBone® SBX Putty ; NanoBone® QD receive FDA 510(k) clearance?

NanoBone® SBX Putty ; NanoBone® QD received FDA 510(k) clearance on 2025-04-07, under 510(k) number K250521.

Who is the listed applicant for NanoBone® SBX Putty ; NanoBone® QD?

The FDA 510(k) record lists Biocomposites, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NanoBone® SBX Putty ; NanoBone® QD?

The FDA product code for NanoBone® SBX Putty ; NanoBone® QD is MQV.

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Other records listing Biocomposites, Ltd. as applicant

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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.

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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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