NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS
K-Number: K024161 · 2003-01-15
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Device Summary
Frequently Asked Questions
What is the NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS?
NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS is a medical device that received FDA 510(k) clearance on 2003-01-15. The listed applicant is Implex Corp.. The 510(k) number is K024161.
When did NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS receive FDA 510(k) clearance?
NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS received FDA 510(k) clearance on 2003-01-15, under 510(k) number K024161.
Who is the listed applicant for NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS?
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 NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS?
The FDA product code for NEXGEN COMPLETE KNEE SOLUTION - TRABECULAR METAL AUGMENTS is JWH.
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: JWH)
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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