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LOSPA IS Spinal System

Corentec Co., Ltd · Model SI.MP6.0022 · UDI-DI 08800068964281

LYQ Prescription
3
510(k) clearances
9
Adverse events
2
Recalls
22
Facilities

Description

Guide Wire

Recalls

DateFirmReason
2017-05-10Zimmer Biomet Spine Inc.Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closur
2015-01-13Medtronic Sofamor Danek USA IncThe product, labeled as containing, one bevel-tipped instrument and one diamond-tipped instrument, may contain either two bevel-tipped instruments or two diamond-tipped instruments

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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.