Oic Variable Angle Small Fragment Locking Plate System

FDA 510(k) K140357 · Orthopaedic Implant Company

Substantially Equivalent

510(k) numberK140357

Submission

Device name
Oic Variable Angle Small Fragment Locking Plate System
Applicant
Orthopaedic Implant Company
Reno, NV, US
Received
February 12, 2014
Decision date
June 9, 2014
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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More from Bonebridge AG

510(k)DeviceDecision
K242995OIC Small / Mini Fragment Plate SystemHRS · Special 10/23/2024SE
K233531OIC FLEX-FIX™ SystemHTN · Traditional 02/02/2024SE
K223761OIC Intramedullary Screw SystemHWC · Traditional 02/13/2023SE
K223118OIC Variable Angle Small Fragment Locking Plate SystemHRS · Traditional 01/21/2023SE
K212601DRPx Locking Distal Radius Plate SystemHRS · Traditional 04/05/2022SE
K202971DRPx Locking Distal Radius Plate SystemHRS · Traditional 05/06/2021SE
K211112OIC External Fixation SystemKTT · Special 05/05/2021SE
K183682OIC External Fixation SystemKTT · Traditional 04/08/2019SE
K182736OIC Suture Anchor SystemMBI · Traditional 12/28/2018SE
K181184OIC Intramedullary Nail SystemHSB · Special 07/27/2018SE

Questions and answers

When was Oic Variable Angle Small Fragment Locking Plate System cleared by the FDA?

Oic Variable Angle Small Fragment Locking Plate System (K140357) received a 510(k) decision of Substantially Equivalent on June 9, 2014, 117 days after the submission was received.

What is the product code of K140357?

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