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ROSA® Knee System

Orthosoft Inc. (d/b/a) Zimmer CAS

Country / Region:Canada (CA)Submission type:Traditional

Product code OLO· 21 CFR 882.4560

Summary PDF

Product code

OLO
21 CFR 882.4560

Predicate devices

1

Cited as predicate

2

Device details

FDA 510(k) registration fields

K number
K221928
Device name
ROSA® Knee System
Country / Region
Canada(CA)
Product code
OLO
Device class
Class 2
Regulation number
21 CFR 882.4560
Date received
2022-07-01
Decision date
2022-10-04
Submission type
Traditional
Technology type
Stereotactic Surgery(AI inferred)
Clinical applications
Knee SurgeryNavigation System
Primary application
Knee Surgery
Classification source
AI classified

Indications for Use

The ROSA Knee System, for use with the ROSA RECON Platform, is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components. The robotic arm placement is performed relative to anatomical landmarks as recorded using the system intraoperatively, and based on a surgical plan optionally determined pre-operatively using compatible X-ray or MRI based surgical planning tools. The ROSA Knee System is designed for use on skeletally mature patient population. The targeted population has the same characteristics as the population that is suitable for the implants compatible with the ROSA Knee System. The ROSA Knee System is to be used with the following fixed bearing knee replacement systems in accordance with their indications and contraindications: NexGen CR, NexGen CR-Flex, NexGen CR-Flex Gender, NexGen LPS, NexGen LPS-Flex, NexGen LPS-Flex Gender, Persona CR, Persona PS, Persona Ti-Nidium CR, Persona Ti-Nidium PS, Persona IQ, Vanguard CR, and Vanguard PS.

Intended Use

The ROSA Knee System, for use with the ROSA RECON Platform, is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon in providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components. The robotic arm placement is performed relative to anatomical landmarks as recorded using the system intraoperatively, and based on a surgical plan optionally determined pre-operatively using compatible X-ray or MRI based surgical planning tools. The ROSA Knee System is designed for use on skeletally mature patient population. The targeted population has the same characteristics as the population that is suitable for the implants compatible with the ROSA Knee System.

Device Description

The ROSA® Knee System for use with the ROSA RECON Platform is used to assist surgeons in performing Total Knee Arthroplasty (TKA) with features to assist with the bone resections as well as assessing the state of the soft tissues to facilitate implant positioning intra-operatively. The ROSA® Knee System uses a Non-Device Medical Device Data System (Non-Device MDDS) called the Zimmer Biomet Drive Portal, which manages the creation and tracking of surgical cases. If the case is image-based, a 3D virtual bone model is generated pre-operatively by the PSI systems (X-PSI Knee System or CAS PSI Knee System) to create a 3D model of the patient's femur/tibia and allows for the preparation of a pre-operative surgical plan. An imageless option is also available where landmarks taken intra-operatively on the patient's bony anatomy are used to create the surgical plan. The intraoperative workflow and surgical concepts implemented in the system remain close to the conventional TKA workflow. The system mainly assists the surgeon in determining reference alignment axes in relation to anatomical landmarks, planning the orthopedic implants location based on these reference alignment axes and orthopedic implant geometry, and precisely positioning the cut guide relative to the planned orthopedic implant location by using a robotic arm.

Summary parsed at:2026-06-24 04:36:21 UTC

Predicate devices

1

K221928 references 1 predicate/reference device

Cited as predicate

2

2 submissions cite K221928 as a predicate