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FDA 510(k)

ILIZAROV DRILL TIP WIRES

K-Number: K130479 · 2013-05-14

ApplicantSmith & Nephew, Inc.
Decision Date2013-05-14
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ILIZAROV DRILL TIP WIRES 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 2013-05-14 under 510(k) number K130479. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILIZAROV DRILL TIP WIRES?

ILIZAROV DRILL TIP WIRES is a medical device that received FDA 510(k) clearance on 2013-05-14. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K130479.

When did ILIZAROV DRILL TIP WIRES receive FDA 510(k) clearance?

ILIZAROV DRILL TIP WIRES received FDA 510(k) clearance on 2013-05-14, under 510(k) number K130479.

Who is the listed applicant for ILIZAROV DRILL TIP WIRES?

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 ILIZAROV DRILL TIP WIRES?

The FDA product code for ILIZAROV DRILL TIP WIRES is KTT.

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Other records listing Smith & Nephew, Inc. as applicant

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Related Devices (Code: KTT)

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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.

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