FDA UDI In Commercial Distribution 🇺🇸 United States

ArTT

DI: 08033390300278 · Model: 8421.15.040 · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ArTT
Primary DI
08033390300278
Version / Model
8421.15.040
Catalog Number
8421.15.040
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-25
Public Version
1
Public Version Date
2025-10-03
Public Version Status
New
Public Device Record Key
e1377341-5f2f-47c7-b711-c8577612ad71

Device Description

Revision Bone Screw - Self-tapping; Dia.6.5mm/L.40mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 08033390300278

Premarket Submissions

Submission Number Supplement Number
K251718 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Dia.6.5mm/L.40mm