Duns Number:432066322
Device Description: SMR Shoulder - Reverse Liner +3 mm Dia. 40 mm - LIMAVIT
Catalog Number
1365.54.815
Brand Name
SMR Shoulder
Version/Model Number
1365.54.815
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
Yes
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
K220792
Product Code
KWS
Product Code Name
Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Public Device Record Key
68bdb67a-6e96-4e56-aa59-09e71aae5913
Public Version Date
July 11, 2022
Public Version Number
1
DI Record Publish Date
July 02, 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 | 595 |
2 | A medical device with a moderate to high risk that requires special controls. | 3634 |