FDA UDI In Commercial Distribution 🇺🇸 United States

Mariner

DI: 10889981182748 · Model: 90-1242 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mariner
Primary DI
10889981182748
Version / Model
90-1242
Catalog Number
90-1242
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-24
Public Version
1
Public Version Date
2019-11-01
Public Version Status
New
Public Device Record Key
920acc14-ec2d-4c04-a699-24f04fde26d8

Device Description

Reduction Screw Driver, Tri-Flat

Device Characteristics

Single Use
No
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
No

Product Codes

Code Name
MNI Orthosis, spinal pedicle fixation
NKB Thoracolumbosacral pedicle screw system
MNH Orthosis, spondylolisthesis spinal fixation
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 10889981182748

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160902 000