Corin MetaFix Hip Stem
K-Number: K162942 · 2017-06-20
Device Summary
Frequently Asked Questions
What is the Corin MetaFix Hip Stem?
Corin MetaFix Hip Stem is a medical device that received FDA 510(k) clearance on 2017-06-20. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K162942.
When did Corin MetaFix Hip Stem receive FDA 510(k) clearance?
Corin MetaFix Hip Stem received FDA 510(k) clearance on 2017-06-20, under 510(k) number K162942.
Who is the listed applicant for Corin MetaFix Hip Stem?
The FDA 510(k) record lists Corin U.S.A. Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Corin MetaFix Hip Stem?
The FDA product code for Corin MetaFix Hip Stem is LZO.
Other records listing Corin U.S.A. Limited 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.