ORTHOLOC™ SPS Shoulder Plating System

FDA 510(k) K191711 · Tornier, Inc.

Substantially Equivalent

510(k) numberK191711

Submission

Device name
ORTHOLOC™ SPS Shoulder Plating System
Applicant
Tornier, Inc.
Bloomington, MN, US
Received
June 26, 2019
Decision date
July 17, 2019
Decision
Substantially Equivalent (SESE)
Type
Special 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 ORTHOLOC™ SPS Shoulder Plating System cleared by the FDA?

ORTHOLOC™ SPS Shoulder Plating System (K191711) received a 510(k) decision of Substantially Equivalent on July 17, 2019, 21 days after the submission was received.

What is the product code of K191711?

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