FDA UDI In Commercial Distribution 🇺🇸 United States

PressON Pedicle Screw System

DI: B678520215S0 · Model: 520215S · NEXUS SPINE, L.L.C.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PressON Pedicle Screw System
Primary DI
B678520215S0
Version / Model
520215S
Company Name
NEXUS SPINE, L.L.C.
Labeler DUNS
028137605
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-31
Public Version
1
Public Version Date
2026-01-08
Public Version Status
New
Public Device Record Key
9d0bfe40-4fc7-4e99-b604-5e7be535e72e

Device Description

MIS Pedicle Screw 5.5 x 25mm, Cannulated

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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary B678520215S0

Premarket Submissions

Submission Number Supplement Number
K160820 000
K223529 000

Device Sizes

Type Value Unit Text
Width 5.5 Millimeter
Length 25 Millimeter