FDA UDI Not in Commercial Distribution 🇺🇸 United States

NorthStar

DI: 10889981196714 · Model: PC1-020015 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NorthStar
Primary DI
10889981196714
Version / Model
PC1-020015
Catalog Number
PC1-020015
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-15
Public Version
2
Public Version Date
2020-12-30
Public Version Status
Update
Public Device Record Key
5b27b71c-6119-4c2e-a0fa-eb3e4b19fdf9
Distribution End Date
2020-12-30

Device Description

Open Lateral Offset, 3.5/ 4.0mm x 15mm

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
NKG Posterior cervical screw system
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

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

Identifiers

Type ID
Primary 10889981196714

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K193615 000