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FDA 510(k)

Stem Extension Line (U2 Total Knee System—PSA Type)

K-Number: K252725 · 2025-09-25

Decision Date2025-09-25
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Stem Extension Line (U2 Total Knee System—PSA Type) is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corporation. It received FDA 510(k) clearance on 2025-09-25 under 510(k) number K252725. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stem Extension Line (U2 Total Knee System—PSA Type)?

Stem Extension Line (U2 Total Knee System—PSA Type) is a medical device that received FDA 510(k) clearance on 2025-09-25. The listed applicant is United Orthopedic Corporation. The 510(k) number is K252725.

When did Stem Extension Line (U2 Total Knee System—PSA Type) receive FDA 510(k) clearance?

Stem Extension Line (U2 Total Knee System—PSA Type) received FDA 510(k) clearance on 2025-09-25, under 510(k) number K252725.

Who is the listed applicant for Stem Extension Line (U2 Total Knee System—PSA Type)?

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

What is the FDA product code for Stem Extension Line (U2 Total Knee System—PSA Type)?

The FDA product code for Stem Extension Line (U2 Total Knee System—PSA Type) is JWH.

Other records listing United Orthopedic Corporation 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 26 devices →

Related Devices (Code: JWH)

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.