FDA 510(k)

SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION

K-Number: K123598 · 2013-06-28

Decision Date2013-06-28

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION 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 2013-06-28 under 510(k) number K123598. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION?

SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 2013-06-28. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K123598.

When did SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION receive FDA 510(k) clearance?

SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION received FDA 510(k) clearance on 2013-06-28, under 510(k) number K123598.

Who is the listed applicant for SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION?

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. HIP SYSTEM INSTRUMENTATION?

The FDA product code for SMITH & NEPHEW, INC. HIP SYSTEM INSTRUMENTATION is JDI.

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Related Devices (Code: JDI)

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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.