Duns Number:313267265
Device Description: OsteoBridge IDSF Diaphysis Femoral Trial Nail 16 130 Connection D: 16 TiAl6V4 ELI non-ster OsteoBridge IDSF Diaphysis Femoral Trial Nail 16 130 Connection D: 16 TiAl6V4 ELI non-sterile
Catalog Number
-
Brand Name
OsteoBridge™
Version/Model Number
GB92417
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
-
Product Code
HWT
Product Code Name
TEMPLATE
Public Device Record Key
3446c832-fecb-419a-ac17-dc2c043b7cab
Public Version Date
October 20, 2022
Public Version Number
2
DI Record Publish Date
November 01, 2021
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 | 328 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1327 |
| U | Unclassified | 13 |