1,671 results · 24ms · Sources: EU EUDAMED, US FDA

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Materialise PKA Guide System

FDA 510(k)
FDA Class 2 ·Orthopedic

Materialise PKA Guide System

FDA 510(k)
FDA Class 2 ·Orthopedic

Materialise PKA Guide System

FDA 510(k)
FDA Class 2 ·Orthopedic

Partial Knee Application (PKA)

FDA 510(k)
FDA Class 2 ·Neurology

NA

FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544050940·Temporary Peek Anatomical Abutment for Int. Hex...

NA

FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544027737·Temporary Peek Anatomical Abutment for Int. Hex...

NA

FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544027744·Temporary Peek Anatomical Abutment for Int. Hex...

RESTORIS PARTIAL KNEE APPLICATION (PKA), RIO STANDARD SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

NA

FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544050933·Abutment Anatomical Peek Int. Hex PM 6x9mm

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·July 8, 2019

3.0 RIO ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·March 26, 2020

MAKO ROBOTIC ARM 3.1

FDA Adverse Event
Injury ·MAKO SURGICAL CORP.·Product code OLO·December 3, 2024

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·August 7, 2019

MAKO ROBOTIC ARM 3.1

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·June 1, 2024

3.0 RIO ROBOTIC ARM - MICS

FDA Adverse Event
Injury ·MAKO SURGICAL CORP.·Product code OLO·May 14, 2020

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·June 18, 2019

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Injury ·MAKO SURGICAL CORP.·Product code OLO·February 20, 2019

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Injury ·MAKO SURGICAL CORP.·Product code OLO·August 29, 2019

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·October 30, 2018

UNKNOWN_MAKO PKA

FDA Adverse Event
Injury ·MAKO SURGICAL CORP.·Product code NPJ·April 26, 2022