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FDA 510(k)

Biomet Kirschner Wires (K-Wires)

K-Number: K241014 · 2024-05-22

ApplicantBiomet, Inc.
Decision Date2024-05-22
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Biomet Kirschner Wires (K-Wires) is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2024-05-22 under 510(k) number K241014. 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 Biomet Kirschner Wires (K-Wires)?

Biomet Kirschner Wires (K-Wires) is a medical device that received FDA 510(k) clearance on 2024-05-22. The listed applicant is Biomet, Inc.. The 510(k) number is K241014.

When did Biomet Kirschner Wires (K-Wires) receive FDA 510(k) clearance?

Biomet Kirschner Wires (K-Wires) received FDA 510(k) clearance on 2024-05-22, under 510(k) number K241014.

Who is the listed applicant for Biomet Kirschner Wires (K-Wires)?

The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Biomet Kirschner Wires (K-Wires)?

The FDA product code for Biomet Kirschner Wires (K-Wires) is HTY.

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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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