FDA UDI In Commercial Distribution 🇺🇸 United States

Apache

DI: M719GHA20240 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Apache
Primary DI
M719GHA20240
Version / Model
1
Catalog Number
GHA-20-24
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
b48dd2a2-bf3d-49dd-a617-9f72c0fcc34f

Device Description

Medium Hyperlordotic ALIF 20mm x 14 DEG

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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary M719GHA20240

Customer Contacts

Phone
512-381-7070

Device Sizes

Type Value Unit Text
Height 20 Millimeter
Angle 24 degree