Integra Proximal Humeral Plate System

FDA 510(k) K121826 · Ascension Orthopedics, Inc.

Substantially Equivalent

510(k) numberK121826

Submission

Device name
Integra Proximal Humeral Plate System
Applicant
Ascension Orthopedics, Inc.
Austin, TX, US
Received
June 21, 2012
Decision date
February 13, 2013
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 Integra Proximal Humeral Plate System cleared by the FDA?

Integra Proximal Humeral Plate System (K121826) received a 510(k) decision of Substantially Equivalent on February 13, 2013, 237 days after the submission was received.

What is the product code of K121826?

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