FDA UDI In Commercial Distribution 🇺🇸 United States

Opticage Expandable Interbody Implant

DI: 81195401112362 · Model: 9080-06 · INTERVENTIONAL SPINE, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Opticage Expandable Interbody Implant
Primary DI
81195401112362
Version / Model
9080-06
Catalog Number
9080-06
Company Name
INTERVENTIONAL SPINE, INC
Labeler DUNS
017663522
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
aeb8b580-ff55-4198-ac1a-685e85186dca

Device Description

11mm Width x 21mm Length by 9mm-14mm Expandable Height

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
MR Safe
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
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 81195401112362

Customer Contacts

Phone
800-497-0484