Catalog Number
88861928-52
Brand Name
Surgilon
Version/Model Number
88861928-52
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 11, 2019
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
K981582,K981582
Product Code
GAR
Product Code Name
SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE
Public Device Record Key
91f2b03c-1409-48a9-be0e-b186ae91375a
Public Version Date
February 05, 2021
Public Version Number
6
DI Record Publish Date
August 31, 2015
Package DI Number
20884521181066
Quantity per Package
24
Contains DI Package
10884521181069
Package Discontinue Date
October 11, 2019
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 |