FDA UDI In Commercial Distribution 🇺🇸 United States

CRESCENT™ Spinal System

DI: 00613994517661 · Model: 7968822 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CRESCENT™ Spinal System
Primary DI
00613994517661
Version / Model
7968822
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0c2b5dd6-04e9-47e8-9140-f8656a6db720

Device Description

ASSEMBLY 7968822 M 37X27 22MM 8 DEG CP

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
MR Conditional
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00613994517661

Customer Contacts

Device Sizes

Type Value Unit Text
Length 37.0 Millimeter
Length 22.0 Millimeter
Height 27.0 Millimeter