Endobutton 7207325
Endobutton 7207325 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K980155 on 1 Apr 1998 and listed in FDA GUDID since 29 Aug 2015 (UDI-DI 03596010388292), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03596010388292 | Date29 Aug 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK980155 | Date1 Apr 1998 | StatusActive |
Official records
- AccessGUDID record 03596010388292
- FDA 510(k) database K980155
Across registries
- FDA 510(k) K980155 decided 1 Apr 1998 Active
- FDA GUDID UDI-DI 03596010388292 listed 29 Aug 2015 Listed
Timeline
- Cleared FDA 510(k) K980155
- Listed FDA GUDID 03596010388292
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Endobutton
- Generic name
- Tendon/ligament bone anchor, non-bioabsorbable
- Model / Ref / Catalog
- 7207325
- Primary DI / UDI-DI
- 03596010388292
- 510(k) Number
- FDA product code
- MBI, GAT
- GMDN term
- Tendon/ligament bone anchor, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040, 878.5000
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Tendon/ligament bone anchor, non-bioabsorbable.
- Interference Screw 909663 by Biomet Orthopedics, Inc.
- BT LOOP BTBXL01709 by S.B.M
- 10008 by Innovate Orthopaedics, Ltd.
- PEEK CF Interference Screw 10166 by PARCUS MEDICAL LLC
- Inion Hexalon™ Biodegradable ACL/PCL Screw ACL-4103 by Inion, Ltd.
- GUARDSMAN C8430 by Conmed Corporation
- Twist PEEK Suture Anchor 10523 by PARCUS MEDICAL LLC
- Arthrex® AR-1588BTB by Arthrex, Inc.
- ToggleLoc With Ziploop 904754 by Biomet Orthopedics, Inc.
- ActivaScrew™ Interference B-AI-0833 by Bioretec Ltd.