Duns Number:942377524
Device Description: Titan™ Humeral Resurfacing ArthroplastyThe Glenoid Retractor is used to facilitate access Titan™ Humeral Resurfacing ArthroplastyThe Glenoid Retractor is used to facilitate access to the joint by withdrawing muscles and tissues for exposure to the joint.
Catalog Number
RET-920-40S
Brand Name
Integra®
Version/Model Number
RET92040S
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
GAD
Product Code Name
RETRACTOR
Public Device Record Key
ce6f1540-8f18-4809-a908-65e128f2b301
Public Version Date
December 14, 2020
Public Version Number
3
DI Record Publish Date
September 29, 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 |