Identity
- Trade Name
- CBYON FDA UDI
- Generic Name
- Multi-purpose stereotactic surgery system FDA UDI
- Device Name
- An electrically-powered computer-aided image-guided stereotactic system that typically consist of a mobile cart or carts, computer, 3D tracking system, surgical instruments that can be tracked, and application software for treatment planning and intraoperative navigation in cranial, ENT, and spine surgical procedures. Intraoperative navigation relies on individual or fused CT and MRI scans registered to the patient to allow the surgeon to correlate the position of navigated instruments used in surgery to the 3D images in real-time. FDA UDI
- Model / Reference
- 90000 FDA UDI
- Description
- An electrically-powered computer-aided image-guided stereotactic system that typically consist of a mobile cart or carts, computer, 3D tracking system, surgical instruments that can be tracked, and application software for treatment planning and intraoperative navigation in cranial, ENT, and spine surgical procedures. Intraoperative navigation relies on individual or fused CT and MRI scans registered to the patient to allow the surgeon to correlate the position of navigated instruments used in surgery to the 3D images in real-time. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860008782700 FDA UDI
- 510(k) Number
- K000171 FDA UDI
- FDA Product Code
- HAW FDA UDI
- GMDN Term
- Multi-purpose stereotactic surgery system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Multi-purpose stereotactic surgery system
Cbyon by Med-Surgical Services — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- NIM-Spine — MEDTRONIC SOFAMOR DANEK, INC. · Class II
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- NAVIGATION ENABLED INSTRUMENTS — MEDOS INTERNATIONAL SARL · Class IIa
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Med-Surgical Services
Sources (1)
- FDA UDI d262ba52-9962-4333-8522-c1b52ace4ba6 34 fields · synced May 30, 2026