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FDA 510(k)

CADIMPLANT

K-Number: K040224 · 2004-04-06

ApplicantPraxim, Inc.
Decision Date2004-04-06
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CADIMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Praxim, Inc.. It received FDA 510(k) clearance on 2004-04-06 under 510(k) number K040224. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CADIMPLANT?

CADIMPLANT is a medical device that received FDA 510(k) clearance on 2004-04-06. The listed applicant is Praxim, Inc.. The 510(k) number is K040224.

When did CADIMPLANT receive FDA 510(k) clearance?

CADIMPLANT received FDA 510(k) clearance on 2004-04-06, under 510(k) number K040224.

Who is the listed applicant for CADIMPLANT?

The FDA 510(k) record lists Praxim, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CADIMPLANT?

The FDA product code for CADIMPLANT is JAK.

Related Clinical Trials

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Related Devices (Code: JAK)

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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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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