FDA UDI In Commercial Distribution 🇺🇸 United States

Dakota ALIF Plate System

DI: 00840019964012 · Model: 69-SD-5020 · PRECISION SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dakota ALIF Plate System
Primary DI
00840019964012
Version / Model
69-SD-5020
Catalog Number
69-SD-5020
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-25
Public Version
3
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
40dc8389-5529-4d82-8a10-90cdcefaa4c3

Device Description

Ø5.0 X 20mm Bone Screw

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
Yes
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

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 00840019964012

Premarket Submissions

Submission Number Supplement Number
K212937 000