FDA UDI In Commercial Distribution 🇺🇸 United States

Lumbar Interbody System

DI: M719GL424H0 · 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
Lumbar Interbody System
Primary DI
M719GL424H0
Version / Model
1
Catalog Number
GL424-H
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-12
Public Version
1
Public Version Date
2024-04-22
Public Version Status
New
Public Device Record Key
9b7753ef-42cd-4bab-b0a2-38805b49da68

Device Description

Hudson Slide Hammer

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
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MQP Spinal Vertebral Body Replacement Device
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
32312 Surgical mallet

Identifiers

Type ID
Primary M719GL424H0

Customer Contacts

Phone
512-381-7070