Ulna Plating System

FDA 510(k) K162424 · Biomet, Inc.

Substantially Equivalent

510(k) numberK162424

Submission

Device name
Ulna Plating System
Applicant
Biomet, Inc.
Warsaw, IN, US
Received
August 30, 2016
Decision date
October 12, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HRS – Plate, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Ulna Plating System cleared by the FDA?

Ulna Plating System (K162424) received a 510(k) decision of Substantially Equivalent on October 12, 2016, 43 days after the submission was received.

What is the product code of K162424?

The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.