FDA UDI In Commercial Distribution 🇺🇸 United States

Rampart One Lumbar Interbody Fusion Device

DI: M7404902108 · Model: 10-10-77-8 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rampart One Lumbar Interbody Fusion Device
Primary DI
M7404902108
Version / Model
10-10-77-8
Catalog Number
490-2108
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
36543a2c-ead8-4a63-ab6a-07db8444c0c6

Device Description

Rampart One Oblique Spacer

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 Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation 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 M7404902108

Customer Contacts

Phone
+1(651)259-8500 ext. 534

Premarket Submissions

Submission Number Supplement Number
K163670 000

Device Sizes

Type Value Unit Text
Height 16 Millimeter