Identity
- Trade Name
- CREO FDA UDI
- Generic Name
- Trans-facet-screw internal spinal fixation system, sterile FDA UDI
- Device Name
- CREO® 5.5, 6.5 - 5.5 x 20mm Cortical Screw FDA UDI
- Model / Reference
- 5119.3522 FDA UDI
- Description
- CREO® 5.5, 6.5 - 5.5 x 20mm Cortical Screw FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00889095113198 FDA UDI
- 510(k) Number
- K124058 FDA UDI
- FDA Product Code
- MNI FDA UDIKWQ FDA UDINKB FDA UDIKWP FDA UDIOSH FDA UDIMNH FDA UDI
- GMDN Term
- Trans-facet-screw internal spinal fixation system, sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI888.3060 FDA UDI888.3050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Dimensions & Sizes
- Size
- Outer Diameter — 6.5 Millimeter FDA UDIOuter Diameter — 5.5 Millimeter FDA UDILength — 20 Millimeter FDA UDI
Category: Trans-facet-screw internal spinal fixation system, sterile
Creo by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Trans-facet-screw internal spinal fixation system, sterile.
- FacetFuse® — SPINEFRONTIER, INC. · U
- CONCERO FACET SCREW SYSTEM — BIOMET SPINE LLC · U
- FacetFuse® — SPINEFRONTIER, INC. · U
- JAZZ System — Implanet · Class II
- Concero™ Facet Screw System — BIOMET SPINE LLC · U
- CREO — GLOBUS MEDICAL, INC. · Class II
- CREO — GLOBUS MEDICAL, INC. · Class II
- SI-LOK — GLOBUS MEDICAL, INC. · Class II
Cleared under the same submission
K124058 also covers:
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, INC.
- CREO — GLOBUS MEDICAL, 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
- Globus Medical, Inc.
Sources (1)
- FDA UDI 67c7b2ea-391d-432a-bc45-f923798941fc 36 fields · synced May 30, 2026