FDA UDI In Commercial Distribution 🇺🇸 United States

Velocity™ Expandable Interbody System

DI: 10840642106916 · Model: 11-2645 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Velocity™ Expandable Interbody System
Primary DI
10840642106916
Version / Model
11-2645
Catalog Number
11-2645
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-25
Public Version
5
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
bea8c982-6167-4051-9f8a-f60e8e3aff99

Device Description

Expandable Implant, 25(L) X 10(W) X 8-14(H) 8 Degree Lordotic

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
61230 Metal-polymer composite spinal interbody fusion cage

Identifiers

Type ID
Primary 10840642106916

Customer Contacts

Phone
203-944-9494

Premarket Submissions

Submission Number Supplement Number
K152620 000

Device Sizes

Type Value Unit Text
Angle 8 degree
Width 10 Millimeter
Length 25 Millimeter
Height 8 Millimeter