FDA UDI In Commercial Distribution 🇺🇸 United States

Flow-Screw™

DI: B267102014500380 · Model: 102-45-0038T · Flow-FX
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Flow-Screw™
Primary DI
B267102014500380
Version / Model
102-45-0038T
Catalog Number
102-45-0038T
Company Name
Flow-FX
Labeler DUNS
079293587
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-30
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
019d39d1-ddea-4161-8429-7abd9396f293

Device Description

SCREW, CANNULATED, (4.5 MM X 38 MM), PARTIALLY THREADED

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary B267102014500380

Premarket Submissions

Submission Number Supplement Number
K142776 000