Duns Number:109903521
Device Description: TWINFIX ULTRA 6.5 MM PK ANCHOR WITH TWO No.2 SUTURES BL TWINFIX ULTRA 6.5 MM PK ANCHOR WITH TWO No.2 SUTURES BLUE, BLUE-COBRAID STERILE
Catalog Number
72203105
Brand Name
TWINFIX
Version/Model Number
72203105
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
MAI
Product Code Name
FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE
Public Device Record Key
4361bdde-8c5d-4c09-b93b-aefa52d5dd78
Public Version Date
November 03, 2020
Public Version Number
6
DI Record Publish Date
August 29, 2015
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 | 10651 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 35590 |
| 3 | A medical device with high risk that requires premarket approval | 351 |