Ecofit® Hip System
K-Number: K163577 · 2017-09-25
Device Summary
Frequently Asked Questions
What is the Ecofit® Hip System?
Ecofit® Hip System is a medical device that received FDA 510(k) clearance on 2017-09-25. The listed applicant is Implantcast GmbH. The 510(k) number is K163577.
When did Ecofit® Hip System receive FDA 510(k) clearance?
Ecofit® Hip System received FDA 510(k) clearance on 2017-09-25, under 510(k) number K163577.
Who is the listed applicant for Ecofit® Hip System?
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 Ecofit® Hip System?
The FDA product code for Ecofit® Hip System 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.