FDA UDI In Commercial Distribution 🇺🇸 United States

Mariner

DI: 10889981146580 · Model: 42-3100 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mariner
Primary DI
10889981146580
Version / Model
42-3100
Catalog Number
42-3100
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
fc2d026c-7f0e-4c2c-9d73-b06f171d8e2c

Device Description

Precontoured ESS PLUS Rod, 6.0 x 100mm

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
KWQ Appliance, fixation, spinal intervertebral body
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Thoracolumbosacral pedicle screw system
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10889981146580

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160902 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 6.0 x 100mm