FDA UDI In Commercial Distribution 🇺🇸 United States

Valeo Spacer System

DI: M555316000204 · Model: A · AMEDICA CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Valeo Spacer System
Primary DI
M555316000204
Version / Model
A
Catalog Number
31-6000-204
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
4
Public Version Date
2018-12-03
Public Version Status
Update
Public Device Record Key
3ba827e1-3c9d-4076-9527-ee536695fe84

Device Description

Tray 1, Phantom Plus PLIF, TLIF System Case 1

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam 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
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary M555316000204

Customer Contacts

Phone
801-839-3500