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ReLine

Nuvasive, Inc. · Model 12355120P · UDI-DI 00887517036216

PMLNKBKWP Prescription
1
510(k) clearances
312
Adverse events (8 deaths)
2
Recalls
80
Facilities

Description

RELINE MAS Ti Rod, 5.5x120mm Straight

Recalls

DateFirmReason
2023-11-28Icotec Agicotec has received notification of one revision that had to be carried out because nut screws had become loose. During the investigation of the device involved, it was detected th
2023-11-28Icotec Agicotec has received notification of one revision that had to be carried out because nut screws had become loose. During the investigation of the device involved, it was detected th

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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.