FDA UDI In Commercial Distribution 🇺🇸 United States

Firebird

DI: 18257200113804 · Model: 44-5690 BE · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Firebird
Primary DI
18257200113804
Version / Model
44-5690 BE
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-21
Public Version
3
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
26728f7e-b668-4108-b9bf-845ba69b3e03

Device Description

6.5MMX90MM MODULAR BONE SCREW SELF-TAPPING

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 Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 18257200113804

Premarket Submissions

Submission Number Supplement Number
K171082 000