FDA UDI In Commercial Distribution 🇺🇸 United States

Epicage Interbody Fusion System

DI: 00844856062801 · Model: 38030-008 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Epicage Interbody Fusion System
Primary DI
00844856062801
Version / Model
38030-008
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
41c4387a-c715-477b-924c-c1efee88368d

Device Description

Epicage Large Spacer - 30mm x 8mm

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
Yes
PM Exempt
No
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 00844856062801

Customer Contacts

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Width 8 Millimeter
Height 8 Millimeter