FDA UDI In Commercial Distribution 🇺🇸 United States

Genesys Spine Apache® Interbody Fusion System

DI: M719GP734140 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genesys Spine Apache® Interbody Fusion System
Primary DI
M719GP734140
Version / Model
1
Catalog Number
GP734-14
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-24
Public Version
1
Public Version Date
2023-08-01
Public Version Status
New
Public Device Record Key
b6a9e786-7892-46fe-bf47-339df74d78f2

Device Description

14mm X 34mm 3DP Parallel TPLIF Ingot Trial

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
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
44788 Spinal implant trial

Identifiers

Type ID
Primary M719GP734140

Customer Contacts

Phone
5123817070

Premarket Submissions

Submission Number Supplement Number
K153123 000

Device Sizes

Type Value Unit Text
Length 34 Millimeter
Width 14 Millimeter