Duns Number:058614483
Device Description: Custom Suture Pack,(4) 88863256-41;(2) 88866307-71;(1) 88868679-01;(2) S-193;(1) S-195;(2) Custom Suture Pack,(4) 88863256-41;(2) 88866307-71;(1) 88868679-01;(2) S-193;(1) S-195;(2) S-608;(1) VP-37-M-X;(2) VP-521-X;(1) VP-705-MX;(1) VP-706-MX
Catalog Number
-
Brand Name
Syneture
Version/Model Number
US1667
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 11, 2021
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
-
Product Code
OVN
Product Code Name
Suture kit
Public Device Record Key
8e779e06-ac97-4f30-83a8-37b921d7f6e5
Public Version Date
February 16, 2021
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
20884521196152
Quantity per Package
6
Contains DI Package
10884521196155
Package Discontinue Date
February 11, 2021
Package Status
Not in Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |