MSS - Humeral reverse liners extension
K-Number: K250338 · 2025-10-31
ApplicantMedacta International S.A.
Decision Date2025-10-31
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MSS - Humeral reverse liners extension is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2025-10-31 under approval number K250338. 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 MSS - Humeral reverse liners extension?
MSS - Humeral reverse liners extension is a medical device that received FDA 510(k) clearance on 2025-10-31. It is manufactured by Medacta International S.A.. The 510(k) number is K250338.
When was MSS - Humeral reverse liners extension approved by the FDA?
MSS - Humeral reverse liners extension received FDA 510(k) clearance on 2025-10-31, under approval number K250338.
What company makes MSS - Humeral reverse liners extension?
MSS - Humeral reverse liners extension is manufactured by Medacta International S.A..
What is the FDA product code for MSS - Humeral reverse liners extension?
The FDA product code for MSS - Humeral reverse liners extension is PHX.
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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.