123 results · 36ms · Sources: EU EUDAMED, US FDA

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WALLFLEX ENTERNAL COLONIC STENT AND ANCHOR LOCK DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 65mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010244·

Arthrex®

FDA UDI
ARTHREX, INC.·00888867522596·Cannulated Canc Screw, FT, 7.0x65mm

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 10, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

NAMILON POWDER

FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI200420650·NAMILON POWDER 16 OZ SHADE 65

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

PATIENT LATEX POLYMER COATED POWDER-FREE GLOVES, CONTAINS 50 MICROGRAM OR LESS OF TOTAL WATER EXTRACTABLE PROTEIN PER GR

FDA 510(k)
FDA Class 1 ·General Hospital

WIENER LAB. CREATININA CINETICA AA

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 4, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 8, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 9, 2019

SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·July 3, 2018

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·October 4, 2017