FDA UDI In Commercial Distribution 🇺🇸 United States

Apache

DI: M719GPC2TI100 · 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
M719GPC2TI100
Version / Model
1
Catalog Number
GPC2Ti-10
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-26
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
47679a63-9032-40a1-b043-e35633bf1045

Device Description

Titanium 25mm Double Convex PLIF

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
61532 Lumbar interspinous decompression spacer, non-sterile

Identifiers

Type ID
Primary M719GPC2TI100

Customer Contacts

Phone
5123817070

Device Sizes

Type Value Unit Text
Height 10 Millimeter