Catalog Number

260-250-940

Brand Name

Healing Abutment

Version/Model Number

260-250-940

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 16, 2019

Issuing Agency

In GS1

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

K092035

Product Code

NHA

Product Code Name

Abutment, Implant, Dental, Endosseous

Public Device Record Key

8406a00d-e816-41a4-a9b2-ceee605784b4

Public Version Date

September 17, 2019

Public Version Number

5

DI Record Publish Date

March 08, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-