FDA UDI In Commercial Distribution 🇺🇸 United States

3DP Lumbar Interbody System

DI: M719GL3DM2040150 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3DP Lumbar Interbody System
Primary DI
M719GL3DM2040150
Version / Model
1
Catalog Number
GL3D-M204015
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-08
Public Version
1
Public Version Date
2020-01-16
Public Version Status
New
Public Device Record Key
a4c43cf5-a834-41cc-80a0-18a8176afaa3

Device Description

Medium 15-Degree 3DP LLIF - 20mm x 40mm

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
57805 Metallic spinal fusion cage, non-sterile

Identifiers

Type ID
Primary M719GL3DM2040150

Customer Contacts

Phone
5123817070

Premarket Submissions

Submission Number Supplement Number
K182987 000

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Height 20 Millimeter
Angle 15 degree