FDA UDI In Commercial Distribution 🇺🇸 United States

SFS;SFS LE;SFS SCOLI

DI: 18257200057733 · Model: 59-3545 · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SFS;SFS LE;SFS SCOLI
Primary DI
18257200057733
Version / Model
59-3545
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-19
Public Version
2
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
53f6f8d6-f9a8-4b40-b8bc-dacedfd4acc2

Device Description

5.5X45 MULTI-AXIAL REDUCTION PEDICLE SCREW

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
Yes
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
MNI Orthosis, spinal pedicle fixation

GMDN Terms

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

Identifiers

Type ID
Primary 18257200057733

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080407 000