FDA UDI In Commercial Distribution 🇺🇸 United States

Complete Cervical

DI: 10889981041014 · Model: 27-14-3513 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Complete Cervical
Primary DI
10889981041014
Version / Model
27-14-3513
Catalog Number
27-14-3513
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
eb7fc953-26a0-4530-87da-c2630e9d9907

Device Description

Screw - Self-Drilling - 3.5x13mm

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
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
57806 Vertebral body prosthesis, non-sterile

Identifiers

Type ID
Primary 10889981041014

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102323 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.5x13mm