FDA UDI In Commercial Distribution 🇺🇸 United States

WAVE D SPINAL SYSTEM

DI: 00643169245150 · Model: 2671211 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WAVE D SPINAL SYSTEM
Primary DI
00643169245150
Version / Model
2671211
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-30
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
73231ac1-b716-4064-9701-2ed728801907

Device Description

DISTRACTOR 2671211 DSTCTR WAVE 11MM12DEG

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00643169245150

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K121333 000

Device Sizes

Type Value Unit Text
Height 11.0 Millimeter
Angle 12.0 degree