UKNEE Tibial insert, posterior stabilized - UKNEE Tibial insert,posterior - UNITED ORTHOPEDIC CORP.

Duns Number:656700556

Device Description: UKNEE Tibial insert,posterior stabilized,small,11mm

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More Product Details

Catalog Number

2301-5111

Brand Name

UKNEE Tibial insert, posterior stabilized

Version/Model Number

2301-5111

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K021657

Product Code Details

Product Code

JWH

Product Code Name

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

Device Record Status

Public Device Record Key

e2cc8e48-0257-4c20-b240-158c32069dec

Public Version Date

July 13, 2018

Public Version Number

4

DI Record Publish Date

October 24, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"UNITED ORTHOPEDIC CORP." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1150
2 A medical device with a moderate to high risk that requires special controls. 4885