Duns Number:942377524
Device Description: Titan™ Total Shoulder SystemIMPACTOR, HEAD, TSSThe Head Impactor is used to properly fit t Titan™ Total Shoulder SystemIMPACTOR, HEAD, TSSThe Head Impactor is used to properly fit the implant and/or trial into the prepared cavity.
Catalog Number
IMP-0920-0795-01
Brand Name
Titan™
Version/Model Number
IP0920079501
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
HWA
Product Code Name
IMPACTOR
Public Device Record Key
a2d6b1c6-9c71-4742-b603-ff40ea8edce1
Public Version Date
July 14, 2020
Public Version Number
3
DI Record Publish Date
September 05, 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 | 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 |