FDA UDI In Commercial Distribution 🇺🇸 United States

Patella Planer

DI: 00819251023276 · Model: 2305.37.000 · TOTAL JOINT ORTHOPEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Patella Planer
Primary DI
00819251023276
Version / Model
2305.37.000
Company Name
TOTAL JOINT ORTHOPEDICS, INC.
Labeler DUNS
078416717
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-25
Public Version
5
Public Version Date
2024-11-13
Public Version Status
Update
Public Device Record Key
1be5565a-96bb-43a4-98ee-11a97029f98e

Device Description

Patella Planer, Size 37

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
No
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00819251023276

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 37

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
The Klassic Knee System should be stored in a clean, dry location at room temperature