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FDA PMA

Prosthesis, hip, semi-constrained, metal/metal, resurfacing

PMA Number: P040033 · 2025-01-10

ApplicantSmith & Nephew, Inc.
Decision Date2025-01-10
PMA NumberP040033
Product CodeNXT
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Prosthesis, hip, semi-constrained, metal/metal, resurfacing is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2025-01-10. The device is classified under product code NXT. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Prosthesis, hip, semi-constrained, metal/metal, resurfacing?

Prosthesis, hip, semi-constrained, metal/metal, resurfacing is a medical device that received FDA 510(k) clearance on 2025-01-10. The listed applicant is Smith & Nephew, Inc..

When did Prosthesis, hip, semi-constrained, metal/metal, resurfacing receive FDA 510(k) clearance?

The clearance date for Prosthesis, hip, semi-constrained, metal/metal, resurfacing can be found in the official FDA records.

Who is the listed applicant for Prosthesis, hip, semi-constrained, metal/metal, resurfacing?

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

What is the FDA product code for Prosthesis, hip, semi-constrained, metal/metal, resurfacing?

The FDA product code for Prosthesis, hip, semi-constrained, metal/metal, resurfacing is NXT.

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.

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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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