Duns Number:263076196
Device Description: TRIAL HUMERAL CUP MOBILITY Ø40+3
Catalog Number
904-0603
Brand Name
Humelock II Cemented Reversible Shoulder
Version/Model Number
904-0603
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
HSD
Product Code Name
Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Public Device Record Key
5365c747-1d02-4ab7-9a95-070149dc263c
Public Version Date
October 07, 2021
Public Version Number
2
DI Record Publish Date
April 18, 2019
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 | 663 |
2 | A medical device with a moderate to high risk that requires special controls. | 478 |