FDA UDI In Commercial Distribution 🇺🇸 United States

iTotal® Patella Sizer

DI: 00850268007170 · Model: 1080-532 · Conformis, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTotal® Patella Sizer
Primary DI
00850268007170
Version / Model
1080-532
Company Name
Conformis, Inc.
Labeler DUNS
808821883
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-24
Public Version
7
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
d06ed14f-8890-42eb-b787-d21e42adb40d

Device Description

iTotal® 41mm Patella Sizer Reusable Instrument

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
Yes
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable
58714 Patella prosthesis trial

Identifiers

Type ID
Primary 00850268007170

Customer Contacts

Phone
781-345-9001

Premarket Submissions

Submission Number Supplement Number
K160025 000

Device Sizes

Type Value Unit Text
Outer Diameter 41 Millimeter