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FDA 510(k)

AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE

K-Number: K131459 · 2013-10-17

ApplicantAap Implantate AG
Decision Date2013-10-17
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2013-10-17 under 510(k) number K131459. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE?

AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE is a medical device that received FDA 510(k) clearance on 2013-10-17. The listed applicant is Aap Implantate AG. The 510(k) number is K131459.

When did AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE receive FDA 510(k) clearance?

AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE received FDA 510(k) clearance on 2013-10-17, under 510(k) number K131459.

Who is the listed applicant for AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE?

The FDA 510(k) record lists Aap Implantate AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE?

The FDA product code for AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE is JDW.

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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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