Duns Number:058311945
Device Description: SPECIALTY TRIATHLON TS TRIAL ASSESSMENT GUIDE SIZE 7 RIGHT
Catalog Number
I-K4275TGR7
Brand Name
SPECIALTY TRIATHLON TS TRIAL ASSESSMENT GUIDE SIZE 7 RIGHT
Version/Model Number
I-K4275TGR7
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
HRY
Product Code Name
PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
Public Device Record Key
abc060f2-d222-49f9-b381-bd8c6cf1b2a2
Public Version Date
March 22, 2022
Public Version Number
2
DI Record Publish Date
February 21, 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 | 5091 |
2 | A medical device with a moderate to high risk that requires special controls. | 10216 |
3 | A medical device with high risk that requires premarket approval | 32 |