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FDA 510(k)

PROCOTYL-E ACETABULAR SYSTEM

K-Number: K043073 · 2005-05-04

Decision Date2005-05-04
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROCOTYL-E ACETABULAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2005-05-04 under 510(k) number K043073. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCOTYL-E ACETABULAR SYSTEM?

PROCOTYL-E ACETABULAR SYSTEM is a medical device that received FDA 510(k) clearance on 2005-05-04. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K043073.

When did PROCOTYL-E ACETABULAR SYSTEM receive FDA 510(k) clearance?

PROCOTYL-E ACETABULAR SYSTEM received FDA 510(k) clearance on 2005-05-04, under 510(k) number K043073.

Who is the listed applicant for PROCOTYL-E ACETABULAR SYSTEM?

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

What is the FDA product code for PROCOTYL-E ACETABULAR SYSTEM?

The FDA product code for PROCOTYL-E ACETABULAR SYSTEM is KWA.

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 Wrightmedicaltechnologyinc 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 268 devices →

Related Devices (Code: KWA)

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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