FDA UDI In Commercial Distribution 🇺🇸 United States

InTess Cervical Cage

DI: B07309CCT64090 · Model: 09-CCT-6409 · Kalitec Direct LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
InTess Cervical Cage
Primary DI
B07309CCT64090
Version / Model
09-CCT-6409
Company Name
Kalitec Direct LLC
Labeler DUNS
041956211
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-13
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
54d470fc-0e53-49e6-9d63-3479233c68e1

Device Description

Cage, 16x14, 9mm 7° TA

Device Characteristics

Single Use
Yes
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B07309CCT64090