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