FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instruments

DI: 00613994503398 · Model: 5220564 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic Reusable Instruments
Primary DI
00613994503398
Version / Model
5220564
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
4e396244-ed83-4208-a123-31462373345d

Device Description

TRASP 5220564 STAND ALONE 16X14 X 5MM

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
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00613994503398

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K073285 000

Device Sizes

Type Value Unit Text
Width 16.0 Millimeter
Outer Diameter 14.0 Millimeter
Height 5.0 Millimeter