AltiVate Reverse® Glenoid
K-Number: K233481 · 2024-05-29
ApplicantEncore Medical L.P.
Decision Date2024-05-29
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
AltiVate Reverse® Glenoid is a medical device manufactured by Encore Medical L.P.. It received FDA 510(k) clearance on 2024-05-29 under approval number K233481. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AltiVate Reverse® Glenoid?
AltiVate Reverse® Glenoid is a medical device that received FDA 510(k) clearance on 2024-05-29. It is manufactured by Encore Medical L.P.. The 510(k) number is K233481.
When was AltiVate Reverse® Glenoid approved by the FDA?
AltiVate Reverse® Glenoid received FDA 510(k) clearance on 2024-05-29, under approval number K233481.
What company makes AltiVate Reverse® Glenoid?
AltiVate Reverse® Glenoid is manufactured by Encore Medical L.P..
What is the FDA product code for AltiVate Reverse® Glenoid?
The FDA product code for AltiVate Reverse® Glenoid is PHX.
Other Devices by Encore Medical L.P.
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K170414Arthrex Univers Revers Apex Humeral StemsArthrex, Inc.
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.