Identity
- Trade Name
- CarboClear Posterior Cervical Screw System FDA UDI
- Generic Name
- General internal orthopaedic fixation system implantation kit FDA UDI
- Device Name
- Probe for use with the CarboClear Posterior Cervical Screw System FDA UDI
- Model / Reference
- Cervical Bone Probe FDA UDI
- Description
- Probe for use with the CarboClear Posterior Cervical Screw System FDA UDI
Identifiers
- Catalog Number
- CS002 FDA UDI
- Primary DI / UDI-DI
- 07290117350928 FDA UDI
- 510(k) Number
- K233989 FDA UDI
- FDA Product Code
- NKG FDA UDIODP FDA UDI
- GMDN Term
- General internal orthopaedic fixation system implantation kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3075 FDA UDI888.3080 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: General internal orthopaedic fixation system implantation kit
CarboClear Posterior Cervical Screw System by Carbofix Orthopedics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General internal orthopaedic fixation system implantation kit.
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Cleared under the same submission
K233989 also covers:
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
- CarboClear Posterior Cervical Screw System — CARBOFIX ORTHOPEDICS LTD
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
- Carbofix Orthopedics Ltd
Sources (1)
- FDA UDI 0c7adab5-afa3-4a17-ba7d-955a6b0a2394 36 fields · synced May 30, 2026