SMITH & NEPHEW MIS HIP STEM
K-Number: K072417 · 2008-01-10
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Device Summary
Frequently Asked Questions
What is the SMITH & NEPHEW MIS HIP STEM?
SMITH & NEPHEW MIS HIP STEM is a medical device that received FDA 510(k) clearance on 2008-01-10. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K072417.
When did SMITH & NEPHEW MIS HIP STEM receive FDA 510(k) clearance?
SMITH & NEPHEW MIS HIP STEM received FDA 510(k) clearance on 2008-01-10, under 510(k) number K072417.
Who is the listed applicant for SMITH & NEPHEW MIS HIP STEM?
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 SMITH & NEPHEW MIS HIP STEM?
The FDA product code for SMITH & NEPHEW MIS HIP STEM is LPH.
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 Smith & Nephew, Inc. 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.
Related Devices (Code: LPH)
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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