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FDA 510(k)

U2 ACETABULAR COMPONENT

K-Number: K050262 · 2005-08-15

Decision Date2005-08-15
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

U2 ACETABULAR COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corp.. It received FDA 510(k) clearance on 2005-08-15 under 510(k) number K050262. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the U2 ACETABULAR COMPONENT?

U2 ACETABULAR COMPONENT is a medical device that received FDA 510(k) clearance on 2005-08-15. The listed applicant is United Orthopedic Corp.. The 510(k) number is K050262.

When did U2 ACETABULAR COMPONENT receive FDA 510(k) clearance?

U2 ACETABULAR COMPONENT received FDA 510(k) clearance on 2005-08-15, under 510(k) number K050262.

Who is the listed applicant for U2 ACETABULAR COMPONENT?

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

What is the FDA product code for U2 ACETABULAR COMPONENT?

The FDA product code for U2 ACETABULAR COMPONENT is LWJ.

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 United Orthopedic 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.

View all 18 devices →

Related Devices (Code: LWJ)

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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