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FDA 510(k)

KIRSCHNER AND GUIDE WIRES

K-Number: K100736 · 2010-09-10

ApplicantSmt Schilling Metalltechnik GmbH
Decision Date2010-09-10
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KIRSCHNER AND GUIDE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Smt Schilling Metalltechnik GmbH. It received FDA 510(k) clearance on 2010-09-10 under 510(k) number K100736. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIRSCHNER AND GUIDE WIRES?

KIRSCHNER AND GUIDE WIRES is a medical device that received FDA 510(k) clearance on 2010-09-10. The listed applicant is Smt Schilling Metalltechnik GmbH. The 510(k) number is K100736.

When did KIRSCHNER AND GUIDE WIRES receive FDA 510(k) clearance?

KIRSCHNER AND GUIDE WIRES received FDA 510(k) clearance on 2010-09-10, under 510(k) number K100736.

Who is the listed applicant for KIRSCHNER AND GUIDE WIRES?

The FDA 510(k) record lists Smt Schilling Metalltechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIRSCHNER AND GUIDE WIRES?

The FDA product code for KIRSCHNER AND GUIDE WIRES is HTY.

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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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