MCP Bone Putty
K-Number: K160446 · 2016-11-07
Device Summary
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. The listed applicant is Biostructures, LLC. The 510(k) number is K160446.
When did MCP Bone Putty receive FDA 510(k) clearance?
MCP Bone Putty received FDA 510(k) clearance on 2016-11-07, under 510(k) number K160446.
Who is the listed applicant for MCP Bone Putty?
The FDA 510(k) record lists Biostructures, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MCP Bone Putty?
The FDA product code for MCP Bone Putty is MQV.
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.