FDA UDI In Commercial Distribution 🇺🇸 United States

CheckMate®

DI: M5284F0110120 · Model: 4F01-1012 · ARTHROSURFACE INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CheckMate®
Primary DI
M5284F0110120
Version / Model
4F01-1012
Catalog Number
4F01-1012
Company Name
ARTHROSURFACE INCORPORATED
Labeler DUNS
144666109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-05
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
7384a4bf-8e4d-4ba9-bff9-f81f0f5f8169

Device Description

Screw, 3.0mm, Locking, 12mm

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

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary M5284F0110120

Customer Contacts

Phone
508-520-3003

Premarket Submissions

Submission Number Supplement Number
K113762 000

Device Sizes

Type Value Unit Text
Length 12 Millimeter