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Altus Spine Interbody Fusion System
FDA UDIClass II (US FDA UDI)
by Altus Spine
Identity
- Trade Name
- Altus Spine Interbody Fusion System FDA UDI
- Generic Name
- Spinal shaver system blade FDA UDI
- Device Name
- Shaver FDA UDI
- Model / Reference
- 1000-0042 FDA UDI
- Description
- Shaver FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00843210130293 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Spinal shaver system blade FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Height — 14 Millimeter FDA UDI
Category: Spinal shaver system blade
Altus Spine Interbody Fusion System by Altus Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Altus Spine
Sources (1)
- FDA UDI bc08995b-7707-46bd-92ce-c6f14bf43201 35 fields · synced Jun 1, 2026