THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330
K-Number: K032344 · 2003-10-02
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Device Summary
Frequently Asked Questions
What is the THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330?
THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330 is a medical device that received FDA 510(k) clearance on 2003-10-02. The listed applicant is Implex Corp.. The 510(k) number is K032344.
When did THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330 receive FDA 510(k) clearance?
THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330 received FDA 510(k) clearance on 2003-10-02, under 510(k) number K032344.
Who is the listed applicant for THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330?
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 MODEL 10-330?
The FDA product code for THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330 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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