Duns Number:942377524
Device Description: The Integra MemoFix staple is a one piece single use nickel titanium alloy bone fixation d The Integra MemoFix staple is a one piece single use nickel titanium alloy bone fixation device intended to be permanently implanted. The device is indicated for the fixation of osteotomies and joint arthrodesis of the hands and feet. The implant consists of two legs connected by a bridge and is offered in multiple combinations of bridge widths and leg lengths to accommodate various anatomies. The system includes instruments, made from titanium and stainless steel, to facilitate the placement of the implants.
Catalog Number
STAPLEIMP
Brand Name
Integra® MemoFix®
Version/Model Number
STAPLEIMP
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
-
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
K123926
Product Code
JDR
Product Code Name
STAPLE, FIXATION, BONE
Public Device Record Key
10133d7e-1afd-43fe-ba67-44fc3ad8aff9
Public Version Date
November 23, 2021
Public Version Number
6
DI Record Publish Date
September 26, 2015
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1909 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1404 |
| 3 | A medical device with high risk that requires premarket approval | 12 |
| U | Unclassified | 15 |