Identity
- Trade Name
- SPIRA-O FDA UDI
- Generic Name
- Bone cutter FDA UDI
- Device Name
- 25° Box Cutter FDA UDI
- Model / Reference
- SPO-111-004 FDA UDI
- Description
- 25° Box Cutter FDA UDI
Identifiers
- Primary DI / UDI-DI
- B030SPO1110040 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone cutter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone cutter
Spira-O by Camber Spine Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Intervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC. · Class I
- Battalion — ALPHATEC SPINE, INC. · Class I
- IdentiTi — ALPHATEC SPINE, INC. · Class I
- Park Dental Research Corp. — Park Dental Research Corp · Class II
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 I | Pending data |
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Manufacturer
- Manufacturer
- Camber Spine Technologies
Sources (1)
- FDA UDI 7c9b6413-2943-47fb-bec2-db12d7ec04c6 34 fields · synced Jun 1, 2026