Duns Number:536935331
Device Description: The trial implant is put in situation to determine the type of correction and to choose th The trial implant is put in situation to determine the type of correction and to choose the final implant. This model is left side, for severe correction.
Catalog Number
-
Brand Name
B-BOP®
Version/Model Number
189030ND
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 22, 2018
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"
Yes
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
5f9f1737-1adf-4834-af4f-2285ace479c8
Public Version Date
March 28, 2019
Public Version Number
4
DI Record Publish Date
May 26, 2017
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 | 388 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 235 |