FDA UDI In Commercial Distribution 🇺🇸 United States

PHOENIX

DI: 18257200029488 · Model: 20-6035 · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PHOENIX
Primary DI
18257200029488
Version / Model
20-6035
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
4
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
73faaf99-a291-462f-83a1-a55bc3e1eb78

Device Description

CoCr Pre-Lordosed Rod w/Hex and Taper, 35mm

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
Yes
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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

Code Name
43257 Bone-screw internal spinal fixation system

Identifiers

Type ID
Primary 18257200029488

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K122901 000

Device Sizes

Type Value Unit Text
Length 35 Millimeter