Duns Number:618749857
Catalog Number
-
Brand Name
GOEZ SCREW 2.0 X 36MM
Version/Model Number
19270
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
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
K081149
Product Code
HWC
Product Code Name
Screw, Fixation, Bone
Public Device Record Key
7b19d910-6f68-44a7-9e25-2a46f1c38913
Public Version Date
June 12, 2019
Public Version Number
1
DI Record Publish Date
June 04, 2019
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 | 494 |
2 | A medical device with a moderate to high risk that requires special controls. | 2447 |