FDA UDI In Commercial Distribution 🇺🇸 United States

SeaSpine Expandable Interbody

DI: 10889981123512 · Model: 82-2612 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SeaSpine Expandable Interbody
Primary DI
10889981123512
Version / Model
82-2612
Catalog Number
82-2612
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-12
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a0b7bf62-bf9d-451a-8771-d1cda060e4f9

Device Description

IMPLANT, 26mm LG, 12-18mm HT, 10mm WD, 0 DEG

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
57806 Vertebral body prosthesis, non-sterile

Identifiers

Type ID
Primary 10889981123512

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133418 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 26mm LG, 12-18mm HT, 10mm WD, 0 Deg