Duns Number:592616445
Device Description: A reusable manual surgical instrument intended to be used during an orthopaedic surgical p A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure
Catalog Number
9095.11.909
Brand Name
Acetabular Retractor Right
Version/Model Number
9095.11.909
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
GAD
Product Code Name
Retractor
Public Device Record Key
067a7d68-dabb-44f8-b1d6-3829a23cc7de
Public Version Date
December 09, 2021
Public Version Number
1
DI Record Publish Date
December 01, 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 | 107 |
2 | A medical device with a moderate to high risk that requires special controls. | 7 |