Identity
- Trade Name
- PYRAMESH® C Titanium Mesh FDA UDI
- Generic Name
- Vertebral body prosthesis FDA UDI
- Device Name
- MESH 9050450 PYRAMESH IMP 10MMX14MMX50MM FDA UDI
- Model / Reference
- 9050450 FDA UDI
- Description
- MESH 9050450 PYRAMESH IMP 10MMX14MMX50MM FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00681490484213 FDA UDI
- 510(k) Number
- K011406 FDA UDI
- FDA Product Code
- MQP FDA UDI
- GMDN Term
- Vertebral body prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3060 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Vertebral body prosthesis
PYRAMESH® C Titanium Mesh by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Vertebral body prosthesis.
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Cleared under the same submission
K011406 also covers:
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, INC.
- PYRAMESH® C Titanium Mesh — MEDTRONIC SOFAMOR DANEK, 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 |
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Manufacturer
- Manufacturer
- Medtronic Sofamor Danek, Inc.
Sources (1)
- FDA UDI 3dbd7ad0-cc09-4537-9187-c1fe1c101f24 36 fields · synced May 30, 2026