FDA 510(k)

SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1

K-Number: K110240 · 2011-04-14

Decision Date2011-04-14

Product CodeOLO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1 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 2011-04-14 under 510(k) number K110240. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1?

SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1 is a medical device that received FDA 510(k) clearance on 2011-04-14. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K110240.

When did SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1 receive FDA 510(k) clearance?

SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1 received FDA 510(k) clearance on 2011-04-14, under 510(k) number K110240.

Who is the listed applicant for SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1?

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. SURESHOT DISTAL TARGETING SYSTEM V2.1?

The FDA product code for SMITH & NEPHEW, INC. SURESHOT DISTAL TARGETING SYSTEM V2.1 is OLO.

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Official Source

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