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FDA 510(k)

SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS

K-Number: K061569 · 2006-07-06

Decision Date2006-07-06
Product CodeNPJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS 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 2006-07-06 under 510(k) number K061569. The device is classified under product code NPJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS?

SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS is a medical device that received FDA 510(k) clearance on 2006-07-06. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K061569.

When did SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS receive FDA 510(k) clearance?

SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS received FDA 510(k) clearance on 2006-07-06, under 510(k) number K061569.

Who is the listed applicant for SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS?

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 COMPETITOR DEUCE FEMORAL COMPONENTS?

The FDA product code for SMITH & NEPHEW COMPETITOR DEUCE FEMORAL COMPONENTS is NPJ.

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.

View all 509 devices →

Related Devices (Code: NPJ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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