Ventix Knotless Anchors
K-Number: K152262 · 2016-03-08
ApplicantBiomet Manufacturing Corp
Decision Date2016-03-08
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Ventix Knotless Anchors is a medical device manufactured by Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2016-03-08 under approval number K152262. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ventix Knotless Anchors?
Ventix Knotless Anchors is a medical device that received FDA 510(k) clearance on 2016-03-08. It is manufactured by Biomet Manufacturing Corp. The 510(k) number is K152262.
When was Ventix Knotless Anchors approved by the FDA?
Ventix Knotless Anchors received FDA 510(k) clearance on 2016-03-08, under approval number K152262.
What company makes Ventix Knotless Anchors?
Ventix Knotless Anchors is manufactured by Biomet Manufacturing Corp.
What is the FDA product code for Ventix Knotless Anchors?
The FDA product code for Ventix Knotless Anchors is MBI.
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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.