FDA UDI In Commercial Distribution 🇺🇸 United States

TRIALTIS

DI: 10705034600055 · Model: 5560-61-6040F · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRIALTIS
Primary DI
10705034600055
Version / Model
5560-61-6040F
Catalog Number
5560616040F
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-17
Public Version
1
Public Version Date
2025-07-25
Public Version Status
New
Public Device Record Key
acb9dccd-f400-44f3-929b-03e85fbf62bb

Device Description

ø5.5-6mm to 6mm x 40mm

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
Yes
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
No

Product Codes

Code Name
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
65114 Bone-screw internal spinal fixation system connector

Identifiers

Type ID
Primary 10705034600055

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242042 000