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CD HORIZON® SOLERA® VOYAGER™ Spinal System

MEDTRONIC SOFAMOR DANEK, INC. · Model X0114263 · UDI-DI 00643169544697

HBE OLO MNI KWQ KWP OSH NKB MNH Prescription

510(k) clearances

22,777

Adverse events (3 deaths)

258

Recalls

140

Facilities

Description

SCREW X0114263 CCM 4.75 XTAB 9.0X65

Recalls

Date	Firm	Reason
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30	SURGIFY MEDICAL OY	Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

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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.