FDA UDI In Commercial Distribution 🇺🇸 United States

GoPLF! Posterior Lateral Fusion System

DI: 07640387660829 · Model: 4010001 · GetSet Surgical SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GoPLF! Posterior Lateral Fusion System
Primary DI
07640387660829
Version / Model
4010001
Company Name
GetSet Surgical SA
Labeler DUNS
480143831
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
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
bb793002-7f5a-4f87-9235-04becf270411

Device Description

The GoPLF! Core instrument set contains instruments numbered 1 – 9 that are placed in chronological order within the tray, for an efficient surgical procedure of the GoPLF! Posterior Lateral Fusion Device (system-specific instruments)

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
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
Primary 07640387660829