MyPAO SA guides
K-Number: K242603 · 2025-11-19
ApplicantMedacta International S.A.
Decision Date2025-11-19
Product CodePBF
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MyPAO SA guides is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2025-11-19 under approval number K242603. The device is classified under product code PBF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MyPAO SA guides?
MyPAO SA guides is a medical device that received FDA 510(k) clearance on 2025-11-19. It is manufactured by Medacta International S.A.. The 510(k) number is K242603.
When was MyPAO SA guides approved by the FDA?
MyPAO SA guides received FDA 510(k) clearance on 2025-11-19, under approval number K242603.
What company makes MyPAO SA guides?
MyPAO SA guides is manufactured by Medacta International S.A..
What is the FDA product code for MyPAO SA guides?
The FDA product code for MyPAO SA guides is PBF.
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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.