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FDA 510(k)

TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ

K-Number: K040630 · 2004-09-30

ApplicantImplex Corp.
Decision Date2004-09-30
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ is the device name listed in this FDA 510(k) record. The listed applicant is Implex Corp.. It received FDA 510(k) clearance on 2004-09-30 under 510(k) number K040630. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ?

TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ is a medical device that received FDA 510(k) clearance on 2004-09-30. The listed applicant is Implex Corp.. The 510(k) number is K040630.

When did TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ receive FDA 510(k) clearance?

TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ received FDA 510(k) clearance on 2004-09-30, under 510(k) number K040630.

Who is the listed applicant for TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ?

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 TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ?

The FDA product code for TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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