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EXPEDIUM VERSE

Medos International Sàrl · Model 199723535 · UDI-DI 10705034403274

PMLMNI Prescription
1
510(k) clearances
310
Adverse events (8 deaths)
2
Recalls
80
Facilities

Description

EXPEDIUM VERSE SPINE SYSTEM FENESTRATED CORTICAL FIX POLYAXIAL SCREW 5.5 5.0 x 35mm

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.