Identity
- Trade Name
- Endoskeleton TAS FDA UDI
- Generic Name
- Metallic spinal interbody fusion cage FDA UDI
- Device Name
- Interbody Fusion Device nanoLOCK Surface Technology 7 Degree Large 10mm FDA UDI
- Model / Reference
- 2307-0210-N FDA UDI
- Description
- Interbody Fusion Device nanoLOCK Surface Technology 7 Degree Large 10mm FDA UDI
Identifiers
- Catalog Number
- 2307-0210-N FDA UDI
- Primary DI / UDI-DI
- M68223070210N0 FDA UDI
- FDA Product Code
- OVD FDA UDI
- GMDN Term
- Metallic spinal interbody fusion cage FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Height — 10 Millimeter FDA UDIWidth — 36 Millimeter FDA UDIDepth — 24 Millimeter FDA UDIAngle — 7 degree FDA UDI
Endoskeleton TAS by Titan Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K111626 also covers:
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS — MEDTRONIC SOFAMOR DANEK, INC.
K141953 also covers:
- ENDOSKELETON® TA nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TAS nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TL nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TO nanoLOCK® Surface Technology — MEDTRONIC SOFAMOR DANEK, INC.
- ENDOSKELETON® TC nanoLOCK® Surface Technology — Titan Spine, Inc.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Titan Spine, Inc.
Sources (1)
- FDA UDI 33d1ffc9-ae2a-4e82-b0fb-d4832c7e2385 38 fields · synced Jun 1, 2026