Actinia® hip stems
K-Number: K232371 · 2023-10-19
Device Summary
Frequently Asked Questions
What is the Actinia® hip stems?
Actinia® hip stems is a medical device that received FDA 510(k) clearance on 2023-10-19. The listed applicant is Implantcast GmbH. The 510(k) number is K232371.
When did Actinia® hip stems receive FDA 510(k) clearance?
Actinia® hip stems received FDA 510(k) clearance on 2023-10-19, under 510(k) number K232371.
Who is the listed applicant for Actinia® hip stems?
The FDA 510(k) record lists Implantcast GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Actinia® hip stems?
The FDA product code for Actinia® hip stems is LZO.
Other records listing Implantcast GmbH 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: LZO)
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.