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FDA 510(k)

RADIAL HEAD IMPLANT

K-Number: K002644 · 2000-11-20

Decision Date2000-11-20
Product CodeKWI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RADIAL HEAD 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 2000-11-20 under 510(k) number K002644. The device is classified under product code KWI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIAL HEAD IMPLANT?

RADIAL HEAD IMPLANT is a medical device that received FDA 510(k) clearance on 2000-11-20. The listed applicant is Avanta Orthopaedics, Inc.. The 510(k) number is K002644.

When did RADIAL HEAD IMPLANT receive FDA 510(k) clearance?

RADIAL HEAD IMPLANT received FDA 510(k) clearance on 2000-11-20, under 510(k) number K002644.

Who is the listed applicant for RADIAL HEAD 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 RADIAL HEAD IMPLANT?

The FDA product code for RADIAL HEAD IMPLANT is KWI.

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 Avanta Orthopaedics, Inc. 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.

View all 18 devices →

Related Devices (Code: KWI)

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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