FDA 510(k)

SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY

K-Number: K082358 · 2008-11-25

Decision Date2008-11-25

Product CodeJWH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY 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 2008-11-25 under 510(k) number K082358. 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 SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY?

SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY is a medical device that received FDA 510(k) clearance on 2008-11-25. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K082358.

When did SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY receive FDA 510(k) clearance?

SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY received FDA 510(k) clearance on 2008-11-25, under 510(k) number K082358.

Who is the listed applicant for SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY?

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, INC. PATIENT MATCHED TECHNOLOGY?

The FDA product code for SMITH & NEPHEW, INC. PATIENT MATCHED TECHNOLOGY is JWH.

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Other records listing Smith & Nephew, Inc. as applicant

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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.