FDA UDI In Commercial Distribution 🇺🇸 United States

Valeo Interbody Fusion Device

DI: M555112091111 · Model: A · AMEDICA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Valeo Interbody Fusion Device
Primary DI
M555112091111
Version / Model
A
Catalog Number
11.209.1111
Company Name
AMEDICA CORPORATION
Labeler DUNS
028629553
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-08
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
b5df7449-8a13-4949-b460-e2d891814c16

Device Description

C+CSC with Lumen 16x12, 0°, 11mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary M555112091111

Customer Contacts

Phone
801-839-3500

Device Sizes

Type Value Unit Text
Width 16 Millimeter
Height 11 Millimeter
Length 12 Millimeter