Ventix Suture Anchor
K-Number: K153558 · 2016-04-21
ApplicantBiomet Manufacturing Corp
Decision Date2016-04-21
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Ventix Suture Anchor is a medical device manufactured by Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2016-04-21 under approval number K153558. 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 Suture Anchor?
Ventix Suture Anchor is a medical device that received FDA 510(k) clearance on 2016-04-21. It is manufactured by Biomet Manufacturing Corp. The 510(k) number is K153558.
When was Ventix Suture Anchor approved by the FDA?
Ventix Suture Anchor received FDA 510(k) clearance on 2016-04-21, under approval number K153558.
What company makes Ventix Suture Anchor?
Ventix Suture Anchor is manufactured by Biomet Manufacturing Corp.
What is the FDA product code for Ventix Suture Anchor?
The FDA product code for Ventix Suture Anchor is MBI.
Related PubMed Literature
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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.