FDA UDI In Commercial Distribution 🇺🇸 United States

Valeo Fusion System

DI: M555110041609 · Model: B · AMEDICA CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Valeo Fusion System
Primary DI
M555110041609
Version / Model
B
Catalog Number
11.004.1609
Company Name
AMEDICA CORPORATION
Labeler DUNS
028629553
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-01
Public Version
5
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
d4efce72-6cef-4324-8288-ce12c2007171

Device Description

Valeo PL,9x21, 6°, 9mm

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary M555110041609

Customer Contacts

Phone
801-839-3500

Device Sizes

Type Value Unit Text
Height 9 Millimeter
Width 21 Millimeter
Length 9 Millimeter