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Wiltrom Spinal Fixation System

WILTROM CO., LTD. · Model 43587555 Polyaxial Reduction Pedicle Screw, Cannulated ø=7.5 L=55 · UDI-DI 04719875729850

NKB Prescription
1
510(k) clearances
24,647
Adverse events (86 deaths)
181
Recalls
409
Facilities

Description

The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments that allow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom Spinal Fixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants are made of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile, and the implants are for single use only.

Recalls

DateFirmReason
2026-05-28SEASPINE ORTHOPEDICS CORPORATIONDue to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
2026-05-22Innovasis, IncPedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with unde
2025-09-19Orthofix U.S. LLCPolyaxial screws do not meet performance standards.
2025-06-30SPINEART SACannulated fenestrated polyaxial screws may be incorrectly labeled
2025-06-30SPINEART SACannulated fenestrated polyaxial screws may be incorrectly labeled
2024-10-29SEASPINE ORTHOPEDICS CORPORATIONDue to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
2024-10-29SEASPINE ORTHOPEDICS CORPORATIONDue to manufacturing defects observed on Locking Caps that affect the ability for components to mate.
2024-08-21XTANT Medical Holdings, IncSpinal fixation system implant screws marked "DNI" are not intended to be implanted and may not have been manufactured in accordance with released manufacturing specifications, and
2024-03-15SPINEART SADue to receiving information regarding difficulties with the insertion of a setscrew inside a screw head. Issues involved, either: 1. The setscrew is not tightened to torque 2. The
2024-02-28SEASPINE ORTHOPEDICS CORPORATIONScrew heads, of pedicle screw systems, have partial thread within the screw head that pose a risk of intraoperative cross-threading within the locking cap/screw head interface.

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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.