Duns Number:313267265
Device Description: OsteoBridge™ OsteoBridge IKA Knee Arthrodesis DIA 40 mm, 10°, l: 50 mm Trial Spacer Screw, OsteoBridge™ OsteoBridge IKA Knee Arthrodesis DIA 40 mm, 10°, l: 50 mm Trial Spacer Screw,non-sterile
Catalog Number
-
Brand Name
OsteoBridge™
Version/Model Number
GA54041-P03
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
4075e9af-fd64-4db0-9295-147c13cf7a1a
Public Version Date
October 13, 2022
Public Version Number
2
DI Record Publish Date
September 05, 2022
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 |