F3D Corpectomy System
FDA 510(k) clearance K202637 · decided 2020-12-23
Clearance details
- K-number
- K202637
- Device name
- F3D Corpectomy System
- Applicant
- Corelink, LLC
- Decision
- Substantially Equivalent
- Date received
- 2020-09-11
- Decision date
- 2020-12-23
- Days to decision
- 103 days
- Clearance type
- Traditional
- Product code
- MQP
- Device class
- 2
- Regulation number
- 888.3060
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- St. Louis, MO, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Vertiwedge® Intraosseous System (K261810) | Foundation Surgical Group | 2026-07-31 |
| POSEIDON ST (K261031) | Signus Medinzintechnik GmbH | 2026-07-10 |
| VyBrate™ VBR System (K253158) | Vy Spine, LLC | 2026-01-07 |
| Vertiwedge® Intraosseous System (K241468) | Foundation Surgical Group, Inc. | 2024-11-07 |
| KONG®-TL VBR System and KONG® C VBR System (K232790) | Icotec AG | 2024-04-04 |
| DOMINION Expandable Corpectomy System (K233359) | Astura Medical | 2024-03-08 |
| VerteLoc Spinal System (K231134) | Signature Orthopaedics Pty, Ltd. | 2024-02-13 |
| Ascend VBR System, Ascend NanoTec VBR System (K232173) | Alphatec Spine, Inc. | 2023-10-06 |
| ArtFx Corpectomy Cages (Espinax and Distractania Corpectomy Cages) (K211892) | Arftx Medical, LLC | 2022-10-06 |
| KONG-TL VBR System, KONG-C VBR System (K200235) | Icotec AG | 2020-05-29 |
| NuVasive X-Core Expandable VBR System, NuVasive X-Core Mini Cervical Expandable VBR System (K193506) | Nu Vasive, Incorporated | 2020-02-26 |
| Small VBR™ (K192117) | Ulrich GmbH & Co. KG | 2019-11-01 |
Recalls involving this device
No recalls on record reference this clearance.