Duns Number:058864308
Device Description: DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot fo DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis
Catalog Number
7125-1818
Brand Name
DynaFORCE™ HiMax
Version/Model Number
DynaFORCE HiMAX Single Packaged Implant 25mm x 18mm x 18mm
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
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
-
Product Code
JDR
Product Code Name
Staple, Fixation, Bone
Public Device Record Key
d277bf5b-e287-43c6-bec6-d32206e68382
Public Version Date
November 23, 2021
Public Version Number
2
DI Record Publish Date
March 20, 2020
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 | 59 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 713 |