RS (Reduced Size) Oss (Orthopedic Salvage System) Additional Components

Q: What is the product code of K051479?

The FDA product code is KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3510.

FDA 510(k) K051479 · Biomet Manufacturing, Inc.

Substantially Equivalent

510(k) numberK051479

Submission

Device name: RS (Reduced Size) Oss (Orthopedic Salvage System) Additional Components
Applicant: Biomet Manufacturing, Inc.
Warsaw, IN, US
Received: June 3, 2005
Decision date: August 10, 2005
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code: KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
Device class: Class II (moderate risk)
Regulation: 21 CFR 888.3510
Specialty: Orthopedic
Implant: Yes

Other 510(k)s with product code KRO

510(k)	Device	Applicant	Decision
K261898	Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee SystemKRO · Traditional	Howmedica Osteonics Corp. dba Stryker Orthopaedics	08/06/2026SE
K252898	Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella…KRO · Traditional	Howmedica Osteonics Corp., Dba Stryker…	12/15/2025SE
K252303	Stem Extension Line (USTAR II System)KRO · Special	United Orthopedic Corporation	08/22/2025SE
K251665	Triathlon® Hinge Knee SystemKRO · Traditional	Howmedica Osteonics Corp., Dba Stryker…	07/25/2025SE
K242871	ATTUNE Revision Hinge KneeKRO · Traditional	Depuy Ireland UC	11/21/2024SE
K240043	EVOLUTION® Hinge Knee System;GUARDIAN limb Salvage System;DCW Modular Distal Femoral…KRO · Traditional	Microport Orthopedics, Inc.	04/01/2024SE
K233980	ATTUNE Total Knee System, ATTUNE Cementless Knee System, LPS Limb Preservation System…KRO · Traditional	Depuy Ireland UC	03/21/2024SE
K230563	EVOLUTION® Hinge Knee SystemKRO · Traditional	Microport Orthopedics, Inc.	09/27/2023SE
K230416	Triathlon® Hinge Knee System; Triathlon® Revision Insert X3®KRO · Traditional	Stryker	05/19/2023SE
K223069	Modular Rotating Hinge Knee Systems and Compatible ComponentsKRO · Traditional	Howmedica Osteonics Corp., Dba Stryker…	04/21/2023SE

More from Howmedica Osteonics Corp., Dba Stryker Orthopaedics

510(k)	Device	Decision
K230540	Patient Specific Planning Solution 3D Bone ModelsLLZ · Traditional	07/25/2023SE
K214001	Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder SystemPHX · Traditional	03/15/2023SE
K211729	Comprehensive® Convertible Glenoid - Vivacit-E LinerPHX · Traditional	11/04/2021SE
K202232	Comprehensive Vault Reconstruction SystemPHX · Traditional	02/19/2021SE
K193038	Comprehensive Shoulder SystemMBF · Traditional	10/28/2020SE
K182516	Comprehensive Nano Stemless ShoulderPKC · Traditional	04/22/2019SE
K181611	Comprehensive Reverse Shoulder SystemPHX · Traditional	09/24/2018SE
K173411	Comprehensive Segmental Revision System (SRS)PHX · Traditional	02/08/2018SE
K172502	Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate…PHX · Traditional	01/03/2018SE
K163651	ExpressBraid Graft ManipulationGAT · Traditional	02/17/2017SE

Questions and answers

When was RS (Reduced Size) Oss (Orthopedic Salvage System) Additional Components cleared by the FDA?

RS (Reduced Size) Oss (Orthopedic Salvage System) Additional Components (K051479) received a 510(k) decision of Substantially Equivalent on August 10, 2005, 68 days after the submission was received.

What is the product code of K051479?

The FDA product code is KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3510.