FDA UDI In Commercial Distribution 🇺🇸 United States

VERTEBRAL SPACER-TR

DI: 10705034800271 · Model: 889.834 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VERTEBRAL SPACER-TR
Primary DI
10705034800271
Version / Model
889.834
Catalog Number
889834
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
7febcfcb-9b14-4a07-8e41-95b662b10c4f

Device Description

VERTEBRAL SPACER-TR 10MMX27MM 7MM HEIGHT

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
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Secondary H9818898340
Primary 10705034800271

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K011037 000