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FacetBRIDGE

LDR Spine Usa, Inc. · Model FS5515T · UDI-DI 03662663026413

MRW Prescription
10
510(k) clearances
105
Adverse events
4
Recalls
100
Facilities

Description

FacetBRIDGE screw D5.5mm L15mm

Recalls

DateFirmReason
2021-04-27Medtronic Sofamor Danek USA, IncProduct is impacted by a thread profile defect due to a manufacturing issue.
2011-06-07Osteomed, LpTwo of the Implant Driver Assembly tips were reported to break during surgery.
2011-03-15Interventional Spine IncThis recall has been initiated due to Pull Pins that may disengage from the Facet Screw during the compression step, requiring that compression be completed with a device driver ra
2011-03-15Interventional Spine IncThis recall has been initiated due to Pull Pins that may disengage from the Facet Screw during the compression step, requiring that compression be completed with a device driver ra

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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.