MONTAGE Settable, Resorbable Bone Putty
K-Number: K222063 · 2023-02-03
ApplicantOrthocon, Inc.
Decision Date2023-02-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MONTAGE Settable, Resorbable Bone Putty is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2023-02-03 under approval number K222063. 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 MONTAGE Settable, Resorbable Bone Putty?
MONTAGE Settable, Resorbable Bone Putty is a medical device that received FDA 510(k) clearance on 2023-02-03. It is manufactured by Orthocon, Inc.. The 510(k) number is K222063.
When was MONTAGE Settable, Resorbable Bone Putty approved by the FDA?
MONTAGE Settable, Resorbable Bone Putty received FDA 510(k) clearance on 2023-02-03, under approval number K222063.
What company makes MONTAGE Settable, Resorbable Bone Putty?
MONTAGE Settable, Resorbable Bone Putty is manufactured by Orthocon, Inc..
What is the FDA product code for MONTAGE Settable, Resorbable Bone Putty?
The FDA product code for MONTAGE Settable, Resorbable Bone Putty is MQV.
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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.