FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOLOC 3DI

DI: 00889797100830 · Model: 58A0X3520 · WRIGHT MEDICAL TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOLOC 3DI
Primary DI
00889797100830
Version / Model
58A0X3520
Catalog Number
58A0X3520
Company Name
WRIGHT MEDICAL TECHNOLOGY, INC.
Labeler DUNS
807201207
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-10
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
8ecf481c-ac63-42d7-aee5-daa7bb24c2c0

Device Description

Plate 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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00889797100830

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152974 000

Device Sizes

Type Value Unit Text
Outer Diameter 3.5 Millimeter
Length 20 Millimeter