FDA UDI In Commercial Distribution 🇺🇸 United States

GoPLF! Posterior Lateral Fusion Device

DI: 07640387660249 · Model: 3201100 · GetSet Surgical SA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
GoPLF! Posterior Lateral Fusion Device
Primary DI
07640387660249
Version / Model
3201100
Company Name
GetSet Surgical SA
Labeler DUNS
480143831
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2023-12-12
Public Version
1
Public Version Date
2023-12-20
Public Version Status
New
Public Device Record Key
7a43ac68-2651-4877-b3b7-4bd132ac5566

Device Description

GoPLF! Posterior Lateral Fusion Device, 5.5mm x 100mm Straight Ti rods-2 per pack

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Unit of Use 07640387660652
Primary 07640387660249