PRO-DENSE LoVisc Bone Graft Substitute
K-Number: K213342 · 2022-01-05
ApplicantWrightmedicaltechnologyinc
Decision Date2022-01-05
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
PRO-DENSE LoVisc Bone Graft Substitute is a medical device manufactured by Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2022-01-05 under approval number K213342. 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 PRO-DENSE LoVisc Bone Graft Substitute?
PRO-DENSE LoVisc Bone Graft Substitute is a medical device that received FDA 510(k) clearance on 2022-01-05. It is manufactured by Wrightmedicaltechnologyinc. The 510(k) number is K213342.
When was PRO-DENSE LoVisc Bone Graft Substitute approved by the FDA?
PRO-DENSE LoVisc Bone Graft Substitute received FDA 510(k) clearance on 2022-01-05, under approval number K213342.
What company makes PRO-DENSE LoVisc Bone Graft Substitute?
PRO-DENSE LoVisc Bone Graft Substitute is manufactured by Wrightmedicaltechnologyinc.
What is the FDA product code for PRO-DENSE LoVisc Bone Graft Substitute?
The FDA product code for PRO-DENSE LoVisc Bone Graft Substitute is MQV.
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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.