Duns Number:107105876
Device Description: MODIFIED INSTRUMENT TLIF SCREW DISTRACTOR
Catalog Number
698344351
Brand Name
NA
Version/Model Number
698344351
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
-
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
GDI
Product Code Name
DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY
Public Device Record Key
78b85a95-8c4a-4c3a-b9f8-80987950eeea
Public Version Date
May 25, 2021
Public Version Number
1
DI Record Publish Date
May 17, 2021
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 | 5839 |
2 | A medical device with a moderate to high risk that requires special controls. | 2784 |
U | Unclassified | 20 |