FDA UDI In Commercial Distribution 🇺🇸 United States

NITRO Interbody Fusion Cage System

DI: 00841732166110 · Model: 213.7332 · CTL Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NITRO Interbody Fusion Cage System
Primary DI
00841732166110
Version / Model
213.7332
Company Name
CTL Medical Corporation
Labeler DUNS
080138504
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-26
Public Version
2
Public Version Date
2025-12-18
Public Version Status
Update
Public Device Record Key
94640f9d-c414-4d01-88c7-c2b88c263526

Device Description

ACIF RASP HEAD, W17xL14, 7DEG, H12mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00841732166110

Customer Contacts

Phone
214-545-5820