FDA UDI In Commercial Distribution 🇺🇸 United States

Rampart One Lumbar Interbody Fusion System

DI: M7404900006 · Model: 49-12-14 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rampart One Lumbar Interbody Fusion System
Primary DI
M7404900006
Version / Model
49-12-14
Catalog Number
490-0006
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-02
Public Version
1
Public Version Date
2019-07-10
Public Version Status
New
Public Device Record Key
d0ec4351-d5c5-4ea9-9eb7-a7102b7192e3

Device Description

Rampart One Inserter Block

Device Characteristics

Single Use
No
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 Unsafe
Direct Marking Exempt
No
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
60847 Polymeric spinal fusion cage, sterile

Identifiers

Type ID
Primary M7404900006

Customer Contacts

Phone
+1(651)256-8500 ext. 513

Premarket Submissions

Submission Number Supplement Number
K191091 000