Duns Number:131747628
Device Description: TKL SPDBRG IMP SYS W/ BC SWVLK & NDL
Catalog Number
AR-2600SBS-11
Brand Name
Arthrex®
Version/Model Number
AR-2600SBS-11
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 26, 2021
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
MAI
Product Code Name
Fastener, fixation, biodegradable, soft tissue
Public Device Record Key
ae0cf09c-9da6-42d4-b456-3ee7d5374eb6
Public Version Date
August 30, 2021
Public Version Number
3
DI Record Publish Date
April 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 | 6506 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 3411 |
| 3 | A medical device with high risk that requires premarket approval | 1 |
| U | Unclassified | 2 |