10,000 results
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89ms
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Sources: EU EUDAMED, US FDA
Medtronic Sofamor Danek USA, Inc.
Manufacturer
🇺🇸 United States·1 Importer
MEDTRONIC SOFAMOR DANEK USA, INC.
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·122 products·🇺🇸 United States
MEDTRONIC SOFAMOR DANEK USA, INC.
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·118 products·🇺🇸 United States
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MJO·April 30, 2014
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MJO·April 30, 2014
ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWQ·April 30, 2014
SOLERA DRIVER 4.75 STANDARD MAS
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC. (MSB)·Product code OLO·July 26, 2016
SOLERA DRIVER 4.75 STANDARD MAS
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC. (MSB)·Product code OLO·September 22, 2015
MICRO PITUITARY
FDA Adverse Event
Injury
·GEBRUEDER ZEPF MEDIZINTECHNIK GMBH & CO. KG·Product code LXH·December 10, 2020
UNKNOWN
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code MAX·February 27, 2023
ORTHOSIS, PEDICLE SPINAL FIXATION
FDA Adverse Event
Injury
·SYNTHES USA·Product code MNI·April 13, 2017
POWEREASE Instruments Set Screw Breakoff Instrument, REF 2346010, Medtronic Sofamor Danek, USA, Inc. Spinal surgical instrumrent.
FDA Enforcement
Class II
·Terminated·Medtronic Sofamor Danek USA Inc·January 21, 2015
SET SCREW RETAINING DRIVER, REF 9010000820, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc. Screwdriver - orthopedic manual surgical instrument.
FDA Enforcement
Class II
·Terminated·Medtronic Sofamor Danek USA Inc·February 5, 2014
ORTHOSIS, SPINE, PLATE,
FDA Adverse Event
Injury
·SYNTHES USA·Product code MNI·November 8, 2016
UNK - PLATES: SPINE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·January 22, 2020
UNK - PLATES: SPINE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·January 22, 2020
UNK - SCREWS
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·January 22, 2020
UNK - SCREWS
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·January 22, 2020
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Enforcement
Class II
·Terminated·Medtronic Sofamor Danek USA Inc·July 3, 2013
INFUSE(R) Bone Graft, LARGE KIT, REF 7510600, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Enforcement
Class II
·Terminated·Medtronic Sofamor Danek USA Inc·July 3, 2013