FDA UDI In Commercial Distribution 🇺🇸 United States

CheckMate®

DI: M5284F0110080 · Model: 4F01-1008 · ARTHROSURFACE INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CheckMate®
Primary DI
M5284F0110080
Version / Model
4F01-1008
Catalog Number
4F01-1008
Company Name
ARTHROSURFACE INCORPORATED
Labeler DUNS
144666109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-14
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
b7a1f56a-bbdb-4f1b-8fc3-d385a1658016

Device Description

Screw, 3.0mm, Locking, 8mm

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
Yes
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
61688 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary M5284F0110080

Customer Contacts

Phone
5085203003

Premarket Submissions

Submission Number Supplement Number
K113762 000