FDA UDI In Commercial Distribution 🇺🇸 United States

PolyLock

DI: 00840124511781 · Model: TN-MB-7033 · FUSION ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PolyLock
Primary DI
00840124511781
Version / Model
TN-MB-7033
Catalog Number
TN-MB-7033
Company Name
FUSION ORTHOPEDICS, LLC
Labeler DUNS
080307067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-10
Public Version
1
Public Version Date
2024-05-20
Public Version Status
New
Public Device Record Key
f3460ff7-3471-4a6d-99d9-72bb400b855f

Device Description

MiniLock Rotation Arm Universal

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
44758 General external orthopaedic fixation system implantation kit, reusable

Identifiers

Type ID
Primary 00840124511781