176 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TRANSCORP SPINAL ACCESS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CapSure® Spine System
FDA UDI
Spine Wave, Inc.·10840642104547·PS3 Screw 10.5mm x 40mm
SIGHT
FDA UDI
FGX INTERNATIONAL INC.·00887661182852·
VERSAFITCUP CC TRIO
FDA 510(k)
FDA Class 2
·Orthopedic
SUMMIT CEMENTED HIP PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
AMISTEM H CEMENTLESS STEM SIZE 2 STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code LZO·December 11, 2014
STEM: AMISTEM H HA COATED STD STEM SIZE 2
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·January 31, 2020
VERSAFITCUP CC TRIO ACETABULAR SHELL CC TRIO Ø 54
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·January 4, 2019
VERSAFITCUP CC TRIO ACETABULAR SHELL
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·August 3, 2017
AMISTEM H, HA COATED STEM SIZE 5 STD
FDA Adverse Event
Death
·MEDACTA INTERNATIONAL SA·Product code LZO·September 20, 2017
AMISTEM H FEMORAL CEMENTLESS STEM SIZE 3 STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code LZO·December 12, 2013
QUADRA-S CEMENTLESS, SAND BLASTED LAT STEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code JDI·July 29, 2015
STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·July 11, 2019
VERSAFITCUP CC CUP IMPACTOR
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL, SA·Product code LXH·November 21, 2014
STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·December 2, 2019
STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 5
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·March 18, 2020
VERSAFITCUP ACETABULAR SHELL CC TRIO Ø 56
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·February 9, 2018
*
FDA Adverse Event
Malfunction
·LINDE GAS NORTH AMERICA LLC·Product code ECX·May 8, 2013
CONSERVE(R) TOTAL A-CLASS HEAD
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JDL·September 24, 2014
PINNACLE SECTOR II CUP 50MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 20, 2011