Duns Number:483016148
Device Description: SELF-DRILLING SCREW, POLYRIGID, Ø4.0 X L14
Catalog Number
TRY-FD 40 14-S
Brand Name
TRYPTIK®2 C-Plate Anterior Cervical Plate System
Version/Model Number
TRY-FD 40 14-S
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 06, 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
-
Product Code
KWQ
Product Code Name
Appliance, Fixation, Spinal Intervertebral Body
Public Device Record Key
40eaba1b-5c3b-4881-9f9c-d08154bb9cd9
Public Version Date
February 21, 2019
Public Version Number
4
DI Record Publish Date
July 12, 2016
Package DI Number
07640151108625
Quantity per Package
2
Contains DI Package
07640151108380
Package Discontinue Date
February 06, 2019
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 974 |
2 | A medical device with a moderate to high risk that requires special controls. | 5209 |