FDA UDI In Commercial Distribution 🇺🇸 United States

Cervical Interbody Spacer Trial

DI: B114210060 · Model: 6mm Trial · CALVARY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cervical Interbody Spacer Trial
Primary DI
B114210060
Version / Model
6mm Trial
Catalog Number
210-06
Company Name
CALVARY SPINE, LLC
Labeler DUNS
832116532
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-01
Public Version
3
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
39c7491f-64fd-401b-9da9-2f9a9a67e04e

Device Description

Trial for 6mm standard cervical inter-vertebral body spacer

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
Yes
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
44788 Spinal implant trial

Identifiers

Type ID
Primary B114210060

Customer Contacts

Phone
786-301-8006

Device Sizes

Type Value Unit Text
Height 6 Millimeter