FDA UDI In Commercial Distribution 🇺🇸 United States

PolyLock Midfoot

DI: 00840124504646 · Model: CD-MF-1040 · FUSION ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PolyLock Midfoot
Primary DI
00840124504646
Version / Model
CD-MF-1040
Catalog Number
CD-MF-1040
Company Name
FUSION ORTHOPEDICS, LLC
Labeler DUNS
080307067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-26
Public Version
2
Public Version Date
2022-03-07
Public Version Status
Update
Public Device Record Key
15f7e43d-d930-4a9a-9ae9-2fa39a0ebe58

Device Description

Calibrated Solid Standard Drill 4.0mm

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
43390 Fluted surgical drill bit, single-use

Identifiers

Type ID
Primary 00840124504646

Premarket Submissions

Submission Number Supplement Number
K202959 000