Duns Number:368715301
Device Description: TorqLoc Interference 9 x 30 mm
Catalog Number
10-1009-0930
Brand Name
TorqLoc Interference
Version/Model Number
10-1009-0930
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K130716
Product Code
MAI
Product Code Name
Fastener, Fixation, Biodegradable, Soft Tissue
Public Device Record Key
6abb2121-340b-4e0e-a723-9846179bddf5
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
February 15, 2017
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 | 142 |
2 | A medical device with a moderate to high risk that requires special controls. | 279 |