APTUS Elbow Dorsal Olecranon Plates
K-Number: K240613 · 2024-06-20
Device Summary
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. The listed applicant is Medartis AG. The 510(k) number is K240613.
When did APTUS Elbow Dorsal Olecranon Plates receive FDA 510(k) clearance?
APTUS Elbow Dorsal Olecranon Plates received FDA 510(k) clearance on 2024-06-20, under 510(k) number K240613.
Who is the listed applicant for APTUS Elbow Dorsal Olecranon Plates?
The FDA 510(k) record lists Medartis AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APTUS Elbow Dorsal Olecranon Plates?
The FDA product code for APTUS Elbow Dorsal Olecranon Plates is HRS.
Other records listing Medartis AG as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.