Surgify Halo (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo (54.070.NVG.H1); Surgify Halo (54.125.NVG.H1); Surgify Halo (54.000.SEE.H1); Surgify Halo (40.070.NVG.H1); Surgify Halo (40.125.NVG.H1); Surgify Halo (40.000.SEE.H1)
FDA 510(k) clearance K251433 · decided 2025-06-04
Clearance details
- K-number
- K251433
- Device name
- Surgify Halo (54.085.SHD.H1); Surgify Halo (54.140.SHD.H1); Surgify Halo (54.070.NVG.H1); Surgify Halo (54.125.NVG.H1); Surgify Halo (54.000.SEE.H1); Surgify Halo (40.070.NVG.H1); Surgify Halo (40.125.NVG.H1); Surgify Halo (40.000.SEE.H1)
- Applicant
- Surgify Medical OY
- Decision
- Substantially Equivalent
- Date received
- 2025-05-08
- Decision date
- 2025-06-04
- Days to decision
- 27 days
- Clearance type
- Special
- Product code
- HBE
- Device class
- 2
- Regulation number
- 882.4310
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Espoo, FI
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trep recall (Z-2558-2026) | SURGIFY MEDICAL OY | 2026-06-24 |
| Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.H1; drills, burrs, trephines recall (Z-2560-2026) | SURGIFY MEDICAL OY | 2026-06-24 |
| Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines recall (Z-2562-2026) | SURGIFY MEDICAL OY | 2026-06-24 |