FDA UDI In Commercial Distribution 🇺🇸 United States

STEALTH™ Anterior Cervical Interbody Spacer

DI: 00840996129374 · Model: D070-1214610 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STEALTH™ Anterior Cervical Interbody Spacer
Primary DI
00840996129374
Version / Model
D070-1214610
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-18
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
9e2150eb-a2dc-4009-87f2-728f0b2bcbd0

Device Description

STEALTH,TRIAL,12X14X10,6 DEG

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00840996129374

Customer Contacts