METAFIX FEMORAL HIP STEM SIZE 1
K-Number: K121439 · 2012-09-14
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Device Summary
Frequently Asked Questions
What is the METAFIX FEMORAL HIP STEM SIZE 1?
METAFIX FEMORAL HIP STEM SIZE 1 is a medical device that received FDA 510(k) clearance on 2012-09-14. The listed applicant is Corin USA. The 510(k) number is K121439.
When did METAFIX FEMORAL HIP STEM SIZE 1 receive FDA 510(k) clearance?
METAFIX FEMORAL HIP STEM SIZE 1 received FDA 510(k) clearance on 2012-09-14, under 510(k) number K121439.
Who is the listed applicant for METAFIX FEMORAL HIP STEM SIZE 1?
The FDA 510(k) record lists Corin USA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for METAFIX FEMORAL HIP STEM SIZE 1?
The FDA product code for METAFIX FEMORAL HIP STEM SIZE 1 is LZO.
Related Clinical Trials
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.
Other records listing Corin USA 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.
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