FDA UDI Not in Commercial Distribution 🇺🇸 United States

PressON™

DI: B6788202220 · Model: 820222 · NEXUS SPINE, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PressON™
Primary DI
B6788202220
Version / Model
820222
Company Name
NEXUS SPINE, L.L.C.
Labeler DUNS
028137605
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-28
Public Version
5
Public Version Date
2023-06-05
Public Version Status
Update
Public Device Record Key
471ff990-7471-45f7-a877-3725a25d543f
Distribution End Date
2023-05-31

Device Description

Push-Release Ratcheting Palm Handle

Device Characteristics

Single Use
No
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Primary B6788202220

Premarket Submissions

Submission Number Supplement Number
K133287 000
K160820 000