THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM
K-Number: K023882 · 2003-02-19
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Device Summary
Frequently Asked Questions
What is the THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM?
THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 2003-02-19. The listed applicant is Implex Corp.. The 510(k) number is K023882.
When did THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM receive FDA 510(k) clearance?
THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM received FDA 510(k) clearance on 2003-02-19, under 510(k) number K023882.
Who is the listed applicant for THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM?
The FDA 510(k) record lists Implex Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM?
The FDA product code for THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM is EZX.
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 Implex Corp. 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: EZX)
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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