Duns Number:107105876
Device Description: MODIFIED INSTRUMENT OSTEOTOME, CURVED 7mm
Catalog Number
698344521
Brand Name
NA
Version/Model Number
698344521
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
HWM
Product Code Name
OSTEOTOME
Public Device Record Key
c7e2c0d2-8d29-4f28-97bd-cde74117cc04
Public Version Date
August 27, 2021
Public Version Number
1
DI Record Publish Date
August 19, 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 |