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FDA 510(k)

MCP Bone Putty

K-Number: K160446 · 2016-11-07

ApplicantBiostructures, LLC
Decision Date2016-11-07
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MCP Bone Putty is a medical device manufactured by Biostructures, LLC. It received FDA 510(k) clearance on 2016-11-07 under approval number K160446. 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 MCP Bone Putty?

MCP Bone Putty is a medical device that received FDA 510(k) clearance on 2016-11-07. It is manufactured by Biostructures, LLC. The 510(k) number is K160446.

When was MCP Bone Putty approved by the FDA?

MCP Bone Putty received FDA 510(k) clearance on 2016-11-07, under approval number K160446.

What company makes MCP Bone Putty?

MCP Bone Putty is manufactured by Biostructures, LLC.

What is the FDA product code for MCP Bone Putty?

The FDA product code for MCP Bone Putty is MQV.

Related Devices (Code: MQV)

K160566Cerasorb Ortho FoamCurasan AG K161351NanoBone SBX PuttyArtoss GmbH K161447HydroSet XTOrthovita, Inc. K152077MaxiGenHans Biomed Corp. K151271BellaFuseHans Biomed Corp. K153608Vitoss BiModal Bone Graft Substitute Foam StripOrthovita, Inc.

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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