FDA UDI In Commercial Distribution 🇺🇸 United States

PressON™

DI: B6785208830 · Model: 520883 · NEXUS SPINE, L.L.C.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PressON™
Primary DI
B6785208830
Version / Model
520883
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
2022-04-30
Public Version
2
Public Version Date
2023-06-09
Public Version Status
Update
Public Device Record Key
d6727b37-d9b8-49d0-a9c1-cd27ab197ff1

Device Description

Max Telescoping Hybrid Coupler 34mm

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

GMDN Terms

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

Identifiers

Type ID
Primary B6785208830

Premarket Submissions

Submission Number Supplement Number
K133287 000
K160820 000

Device Sizes

Type Value Unit Text
Length 34 Millimeter