Identity
- Trade Name
- obeliscPRO™ vertebral body replacement FDA UDI
- Generic Name
- Vertebral body prosthesis FDA UDI
- Device Name
- obelisc lateral end piece, green, length 45 mm, angle 15° FDA UDI
- Model / Reference
- CS 2915-15 FDA UDI
- Description
- obelisc lateral end piece, green, length 45 mm, angle 15° FDA UDI
Identifiers
- Catalog Number
- CS 2915-15 FDA UDI
- Primary DI / UDI-DI
- 04052536113774 FDA UDI
- 510(k) Number
- K060416 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
MR Conditional FDA UDI
Category: Vertebral body prosthesis
obeliscPRO™ vertebral body replacement by Ulrich GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vertebral body prosthesis.
- CASCADIA™ Interbody System — K2M, INC. · Class II
- CHESAPEAKE® Stabilization System — K2M, INC. · Class II
- CASCADIA™ Interbody System — K2M, INC. · Class II
- FORTIFY — GLOBUS MEDICAL, INC. · Class II
- VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
- CASCADIA™ Interbody System — K2M, INC. · Class II
- CAPRI™ Corpectomy Cage System — K2M, INC. · Class II
- Cascadia™ Interbody System — K2M, INC. · Class II
Cleared under the same submission
K060416 also covers:
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obeliscPRO™ vertebral body replacement — Ulrich GmbH & Co. KG
- obelisc™ vertebral body replacement — Ulrich GmbH & Co. KG
- obelisc™ vertebral body replacement — Ulrich GmbH & Co. KG
- obelisc™ vertebral body replacement — Ulrich GmbH & Co. KG
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
- Ulrich GmbH & Co. KG
Sources (1)
- FDA UDI a18147a9-e6fc-4182-87f7-0d3a97f78afa 36 fields · synced Jun 8, 2026