Biomet Proximal Humerus Plating System

FDA 510(k) K143697 · Biomet Manufacturing

Substantially Equivalent

510(k) numberK143697

Submission

Device name
Biomet Proximal Humerus Plating System
Applicant
Biomet Manufacturing
Warsaw, IN, US
Received
December 24, 2014
Decision date
March 30, 2015
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 Biomet Proximal Humerus Plating System cleared by the FDA?

Biomet Proximal Humerus Plating System (K143697) received a 510(k) decision of Substantially Equivalent on March 30, 2015, 96 days after the submission was received.

What is the product code of K143697?

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