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Name Classification Manufacturer Risk Class Country Source
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW Orthopedic Devices SPINEART SA 2 United States USFDA
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW Orthopedic Devices SPINEART SA 2 United States USFDA
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW Orthopedic Devices SPINEART SA 2 United States USFDA
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW 4.0 MM, 04 L14, REF TRYPS40 14S Orthopedic Devices SPINEART SA 2 United States USFDA
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW Orthopedic Devices SPINEART SA 2 United States USFDA
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW Orthopedic Devices SPINEART SA 2 United States USFDA
Device Recall TRYPTIK(R) 2 CPLATE SELFTAPPING POLYAXIAL SCREW Orthopedic Devices SPINEART SA 2 United States USFDA