FDA UDI In Commercial Distribution 🇺🇸 United States

CarboClear Lumbar Cage System

DI: 07290110206871 · Model: Implant Trial-10x23x14mm · CARBOFIX ORTHOPEDICS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CarboClear Lumbar Cage System
Primary DI
07290110206871
Version / Model
Implant Trial-10x23x14mm
Catalog Number
CCLC02314
Company Name
CARBOFIX ORTHOPEDICS LTD
Labeler DUNS
649185170
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-28
Public Version
1
Public Version Date
2020-06-05
Public Version Status
New
Public Device Record Key
78f48d94-7821-4995-a1d9-a8d1da529703

Device Description

A surgical tool for use with the lumbar intervertebral body fusion device (cage). The Implant Trial is intended for use before insertion of the implant into the intervertebral space, to assist in selection of correct implant dimensions and to verify implant position within the disc space.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 07290110206871

Customer Contacts

Phone
+97299511511

Premarket Submissions

Submission Number Supplement Number
K193378 000