Osteo-P Bone Graft Substitute
K-Number: K170165 · 2017-12-29
ApplicantMolecular Matrix, Inc.
Decision Date2017-12-29
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Osteo-P Bone Graft Substitute is a medical device manufactured by Molecular Matrix, Inc.. It received FDA 510(k) clearance on 2017-12-29 under approval number K170165. 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 Osteo-P Bone Graft Substitute?
Osteo-P Bone Graft Substitute is a medical device that received FDA 510(k) clearance on 2017-12-29. It is manufactured by Molecular Matrix, Inc.. The 510(k) number is K170165.
When was Osteo-P Bone Graft Substitute approved by the FDA?
Osteo-P Bone Graft Substitute received FDA 510(k) clearance on 2017-12-29, under approval number K170165.
What company makes Osteo-P Bone Graft Substitute?
Osteo-P Bone Graft Substitute is manufactured by Molecular Matrix, Inc..
What is the FDA product code for Osteo-P Bone Graft Substitute?
The FDA product code for Osteo-P 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.