FDA UDI In Commercial Distribution 🇺🇸 United States

Balanced Knee System

DI: 00822409009282 · Model: 163-1716 · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Balanced Knee System
Primary DI
00822409009282
Version / Model
163-1716
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
bdd795a1-b140-4fe5-8d3e-7f30d38fa19a

Device Description

Size 7 16mm Tibial Insert PS

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 00822409009282

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K994370 000

Device Sizes

Type Value Unit Text
Height 16 Millimeter