8 results
·
72ms
·
Sources: EU EUDAMED, US FDA
NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
FDA Recall
Terminated
·Blue Belt Technologies MN·Product code OLO·April 11, 2014
Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.
FDA Recall
Terminated
·Blue Belt Technologies MN·Product code KKX·July 19, 2013
Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
FDA Recall
Terminated
·Blue Belt Technologies MN·Product code HSX·June 4, 2014
Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
FDA Recall
Terminated
·Blue Belt Technologies MN·Product code HSX·June 4, 2014
NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·May 21, 2014
Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·July 9, 2014
Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·July 9, 2014
Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.
FDA Enforcement
Class II
·Terminated·Blue Belt Technologies MN·August 28, 2013