FDA Device Intelligence
HomeMEDTRONIC SOFAMOR DANEK, INC. › Translace™ Spinal Tethering System

Translace™ Spinal Tethering System

MEDTRONIC SOFAMOR DANEK, INC. · Model 9010007012 · UDI-DI 00763000333386

OWI Prescription
1
510(k) clearances
68
Adverse events
2
Recalls
64
Facilities

Description

TETHER 9010007012 0.2MM INSERT ASSEMBLY

Recalls

DateFirmReason
2020-10-08Medicrea InternationalTightening the LIGAPASS Band with this instrument, the tensioner's pliers can crush the band causing the band to break during surgery and lead to a risk of infection and re-interv
2017-04-24OrthoPediatrics CorpOver-tensioning of the band resulting in damage to the band causing it to rupture

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.