FDA UDI In Commercial Distribution 🇺🇸 United States

Preference

DI: 00841732152076 · Model: 28-7201-090 · CTL Medical Corporation
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Preference
Primary DI
00841732152076
Version / Model
28-7201-090
Company Name
CTL Medical Corporation
Labeler DUNS
080138504
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-31
Public Version
1
Public Version Date
2024-11-08
Public Version Status
New
Public Device Record Key
4feed912-353c-4237-8e92-b6b14ddafee6

Device Description

7.2mm Polyaxial Screw Reduction 90mm Green

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
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
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00841732152076

Customer Contacts

Phone
214-545-5820

Premarket Submissions

Submission Number Supplement Number
K081296 000