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Synthes GmbH · Model A-CRN-S-G1 · UDI-DI 00845384012597

HBE Prescription
1
510(k) clearances
22,777
Adverse events (3 deaths)
258
Recalls
140
Facilities

Description

2.15 mm x 22 mm Fluted Spiral Router. Use with CRANI-A-G1, CRANI-A-R-G1, CRANI-A, CRANI-A-R Attachments.

Recalls

DateFirmReason
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
2026-04-30SURGIFY MEDICAL OYPotential 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.