EcoFit Vit E Acetabular System
K-Number: K180263 · 2018-07-20
Device Summary
Frequently Asked Questions
What is the EcoFit Vit E Acetabular System?
EcoFit Vit E Acetabular System is a medical device that received FDA 510(k) clearance on 2018-07-20. The listed applicant is Implantcast GmbH. The 510(k) number is K180263.
When did EcoFit Vit E Acetabular System receive FDA 510(k) clearance?
EcoFit Vit E Acetabular System received FDA 510(k) clearance on 2018-07-20, under 510(k) number K180263.
Who is the listed applicant for EcoFit Vit E Acetabular 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 Vit E Acetabular System?
The FDA product code for EcoFit Vit E Acetabular 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.