FDA recall Z-2108-2018

MEDTECH SAS · Class II · device

Product

ROSA(TM) Robotized Stereotactic Assistant, Version 2.5 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgical condition in which the use of stereotactic surgery may be appropriate.

Reason for recall

Replacement of units lacking an updated device approval.

Distribution

US Distribution

Key facts

Status
Terminated
Initiation date
2018-05-08
Report date
2018-06-13
Termination date
2020-08-19
Voluntary/Mandated
Voluntary: Firm initiated
Location
Montpellier, N/A, France

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2108-2018