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FDA 510(k)

WRIST IMPLANT

K-Number: K021859 · 2002-12-02

ApplicantAvanta Orthopaedics, Inc.
Decision Date2002-12-02
Product CodeJWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WRIST IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Avanta Orthopaedics, Inc.. It received FDA 510(k) clearance on 2002-12-02 under 510(k) number K021859. The device is classified under product code JWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIST IMPLANT?

WRIST IMPLANT is a medical device that received FDA 510(k) clearance on 2002-12-02. The listed applicant is Avanta Orthopaedics, Inc.. The 510(k) number is K021859.

When did WRIST IMPLANT receive FDA 510(k) clearance?

WRIST IMPLANT received FDA 510(k) clearance on 2002-12-02, under 510(k) number K021859.

Who is the listed applicant for WRIST IMPLANT?

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

What is the FDA product code for WRIST IMPLANT?

The FDA product code for WRIST IMPLANT is JWJ.

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Other records listing Avanta Orthopaedics, Inc. as applicant

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Related Devices (Code: JWJ)

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

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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