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FDA 510(k)

LEGION STEM WITH HOLES

K-Number: K072531 · 2007-12-06

Decision Date2007-12-06
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LEGION STEM WITH HOLES 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 2007-12-06 under 510(k) number K072531. 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 LEGION STEM WITH HOLES?

LEGION STEM WITH HOLES is a medical device that received FDA 510(k) clearance on 2007-12-06. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K072531.

When did LEGION STEM WITH HOLES receive FDA 510(k) clearance?

LEGION STEM WITH HOLES received FDA 510(k) clearance on 2007-12-06, under 510(k) number K072531.

Who is the listed applicant for LEGION STEM WITH HOLES?

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 LEGION STEM WITH HOLES?

The FDA product code for LEGION STEM WITH HOLES is JWH.

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: 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

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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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