Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
PMA Number: P150030 · 2025-04-17
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Device Summary
Frequently Asked Questions
What is the Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented?
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is a medical device that received FDA 510(k) clearance on 2025-04-17. The listed applicant is Smith & Nephew, Inc..
When did Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented receive FDA 510(k) clearance?
The clearance date for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented can be found in the official FDA records.
Who is the listed applicant for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented?
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/ceramic/ceramic/metal, cemented or uncemented?
The FDA product code for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is MRA.
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.
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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