JuggerKnot Soft Anchor SSI002542
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00880304858985 | Date16 Feb 2017 | StatusListed |
Recalls
-
- Terminated Z-3252-2018
Expiration date incorrectly listed on the label
-
- Terminated Z-1828-2016
Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.
-
- Terminated Z-3109-2011
The device packaging was punctured by the device, resulting in loss of implant sterility.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- JuggerKnot Soft Anchor
- Generic Name
- Surgical drill guide, reusable
- Model / Ref / Catalog
- SSI002542
- Primary DI / UDI-DI
- 00880304858985
- 510(k) Number
- FDA Product Code
- MBI
- GMDN Term
- Surgical drill guide, reusable
- Device Class
- Class II
- Regulation Number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Biomet Orthopedics, Inc.
Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No