FDA UDI Not in Commercial Distribution 🇺🇸 United States

MONDRIAN PLIF

DI: 00841732150980 · Model: 127.1187 · CTL Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MONDRIAN PLIF
Primary DI
00841732150980
Version / Model
127.1187
Company Name
CTL Medical Corporation
Labeler DUNS
080138504
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-29
Public Version
4
Public Version Date
2026-04-01
Public Version Status
Update
Public Device Record Key
0999ac23-69ba-4a89-9ddd-dabdb6d26e13
Distribution End Date
2026-03-31

Device Description

MONDRIAN PLIF Cage, Straight, Titanium feat TiCro, 15 Deg, W9xL22, H7mm

Device Characteristics

Single Use
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00841732150980

Customer Contacts

Phone
214-545-5820

Premarket Submissions

Submission Number Supplement Number
K192863 000