FDA UDI In Commercial Distribution 🇺🇸 United States

Valeo Interbody Fusion System

DI: M555123011513 · Model: D · AMEDICA CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Valeo Interbody Fusion System
Primary DI
M555123011513
Version / Model
D
Catalog Number
12.301.1513
Company Name
AMEDICA CORPORATION
Labeler DUNS
028629553
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-29
Public Version
5
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
c7c54be3-75db-46d8-96ee-6a1f7bd22686

Device Description

Valeo II PL 11x23 5°, 13mm

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary M555123011513

Customer Contacts

Phone
801-839-3500

Device Sizes

Type Value Unit Text
Length 23 Millimeter
Height 13 Millimeter
Width 11 Millimeter