AltiVate® Anatomic Shoulder AG e+ with Markers
K-Number: K222592 · 2023-06-23
ApplicantEncore Medical L.P.
Decision Date2023-06-23
Product CodeKWS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
AltiVate® Anatomic Shoulder AG e+ with Markers is a medical device manufactured by Encore Medical L.P.. It received FDA 510(k) clearance on 2023-06-23 under approval number K222592. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AltiVate® Anatomic Shoulder AG e+ with Markers?
AltiVate® Anatomic Shoulder AG e+ with Markers is a medical device that received FDA 510(k) clearance on 2023-06-23. It is manufactured by Encore Medical L.P.. The 510(k) number is K222592.
When was AltiVate® Anatomic Shoulder AG e+ with Markers approved by the FDA?
AltiVate® Anatomic Shoulder AG e+ with Markers received FDA 510(k) clearance on 2023-06-23, under approval number K222592.
What company makes AltiVate® Anatomic Shoulder AG e+ with Markers?
AltiVate® Anatomic Shoulder AG e+ with Markers is manufactured by Encore Medical L.P..
What is the FDA product code for AltiVate® Anatomic Shoulder AG e+ with Markers?
The FDA product code for AltiVate® Anatomic Shoulder AG e+ with Markers is KWS.
Related Clinical Trials
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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.