FDA UDI In Commercial Distribution 🇺🇸 United States

3DP Lumbar Interbody System

DI: M719GLL103M0800SST0 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
3DP Lumbar Interbody System
Primary DI
M719GLL103M0800SST0
Version / Model
1
Catalog Number
GLL103-M0800S-ST
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-12
Public Version
1
Public Version Date
2024-12-20
Public Version Status
New
Public Device Record Key
2e8ef9c5-3605-4366-b2ed-a87339fdc18a

Device Description

LLIF Angled Rasp, 8mm x 0-Degree, Stick Rasp

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical
MQP Spinal Vertebral Body Replacement Device
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary M719GLL103M0800SST0

Customer Contacts

Phone
512-381-7070