FDA UDI In Commercial Distribution 🇺🇸 United States

NewPort

DI: 10889981135898 · Model: 64-7560 · Seaspine Orthopedics Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NewPort
Primary DI
10889981135898
Version / Model
64-7560
Catalog Number
64-7560
Company Name
Seaspine Orthopedics Corporation
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-11
Public Version
3
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
e41ba4ed-f143-40ee-8c6a-2b6df2c8fff1

Device Description

NewPort 4mm Hex Screw, Ø7.5 x 60mm

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
MNH Orthosis, spondylolisthesis spinal fixation
MNI Orthosis, spinal pedicle fixation
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 10889981135898

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K161535 000

Device Sizes

Type Value Unit Text
Device Size Text, specify DIA7.5 x 60mm