FDA UDI In Commercial Distribution 🇺🇸 United States

Abacus® Spacer System

DI: 10840642102444 · Model: 11-9058 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Abacus® Spacer System
Primary DI
10840642102444
Version / Model
11-9058
Catalog Number
11-9058
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d61390a6-645b-4dba-b359-6c10582ce9df

Device Description

Lordotic Implant 60x18x14mm 10deg

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
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary 10840642102444

Customer Contacts

Phone
203-944-9494

Premarket Submissions

Submission Number Supplement Number
K140007 000

Device Sizes

Type Value Unit Text
Width 18 Millimeter
Height 14 Millimeter
Length 60 Millimeter
Angle 10 degree