APTUS Elbow Dorsal Olecranon Plates
K-Number: K240613 · 2024-06-20
ApplicantMedartis AG
Decision Date2024-06-20
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
APTUS Elbow Dorsal Olecranon Plates is a medical device manufactured by Medartis AG. It received FDA 510(k) clearance on 2024-06-20 under approval number K240613. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the APTUS Elbow Dorsal Olecranon Plates?
APTUS Elbow Dorsal Olecranon Plates is a medical device that received FDA 510(k) clearance on 2024-06-20. It is manufactured by Medartis AG. The 510(k) number is K240613.
When was APTUS Elbow Dorsal Olecranon Plates approved by the FDA?
APTUS Elbow Dorsal Olecranon Plates received FDA 510(k) clearance on 2024-06-20, under approval number K240613.
What company makes APTUS Elbow Dorsal Olecranon Plates?
APTUS Elbow Dorsal Olecranon Plates is manufactured by Medartis AG.
What is the FDA product code for APTUS Elbow Dorsal Olecranon Plates?
The FDA product code for APTUS Elbow Dorsal Olecranon Plates is HRS.
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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.