EcoFit Vit E Acetabular System
K-Number: K180263 · 2018-07-20
ApplicantImplantcast GmbH
Decision Date2018-07-20
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
EcoFit Vit E Acetabular System is a medical device manufactured by Implantcast GmbH. It received FDA 510(k) clearance on 2018-07-20 under approval number K180263. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Implantcast GmbH. The 510(k) number is K180263.
When was EcoFit Vit E Acetabular System approved by the FDA?
EcoFit Vit E Acetabular System received FDA 510(k) clearance on 2018-07-20, under approval number K180263.
What company makes EcoFit Vit E Acetabular System?
EcoFit Vit E Acetabular System is manufactured by Implantcast GmbH.
What is the FDA product code for EcoFit Vit E Acetabular System?
The FDA product code for EcoFit Vit E Acetabular System is LZO.
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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.