FDA UDI In Commercial Distribution 🇺🇸 United States

Mariner Outrigger

DI: 10889981176013 · Model: 99-1130-320 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mariner Outrigger
Primary DI
10889981176013
Version / Model
99-1130-320
Catalog Number
99-1130-320
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-30
Public Version
1
Public Version Date
2019-08-07
Public Version Status
New
Public Device Record Key
b628526a-171d-450d-bde4-6546f6edfae5

Device Description

Z-Rod, Dia. 6.0mm, Titanium, 320mm

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

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

Identifiers

Type ID
Primary 10889981176013

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183639 000