FDA UDI In Commercial Distribution 🇺🇸 United States

DYNA-LOK® Spinal System

DI: 00673978150864 · Model: X1096-035 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DYNA-LOK® Spinal System
Primary DI
00673978150864
Version / Model
X1096-035
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-18
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
5a02e0cf-aea8-4d4e-8f74-256fa77ba5a2

Device Description

DYN 10-32 NUT TI

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
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 00673978150864

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K936307 000