Duns Number:058614483
Device Description: Braided Absorbable Suture
Catalog Number
-
Brand Name
Polysorb
Version/Model Number
GL72MG
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 21, 2022
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
K963253,K963253
Product Code
GAM
Product Code Name
SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
Public Device Record Key
868d30b4-ddc0-4a99-897d-3c07fd4d19d6
Public Version Date
August 08, 2022
Public Version Number
9
DI Record Publish Date
October 11, 2017
Package DI Number
20884521724607
Quantity per Package
12
Contains DI Package
10884521724600
Package Discontinue Date
July 21, 2022
Package Status
Not in Commercial Distribution
Package Type
PACK_OR_INNER_PACK
| 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 |