FlareHawk Interbody Fusion System
FDA 510(k) K202198 · Integrity Implants, Inc.
510(k) numberK202198
Submission
- Device name
- FlareHawk Interbody Fusion System
- Applicant
- Integrity Implants, Inc.
Palm Beach Gardens, FL, US - Received
- August 5, 2020
- Decision date
- November 3, 2020
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MAX – Intervertebral Fusion Device With Bone Graft, Lumbar
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3080
- Specialty
- Orthopedic
- Implant
- Yes
Intended to stabilize spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.
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|---|---|---|---|
| K261049 | Scala® TLMAX · Traditional | Spineart SA | 08/20/2026SE |
| K261430 | TruLift Expandable SystemMAX · Traditional | Life Spine, Inc. | 07/28/2026SE |
| K253011 | Catalyft PL Expandable Interbody SystemMAX · Traditional | Medtronic Sofamor Danek USA, Inc. | 07/17/2026SE |
| K261020 | Symmetrix L Spinal SystemMAX · Traditional | Medtronic Sofamor Danek USA, Inc. | 07/14/2026SE |
| K253420 | Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer…MAX · Traditional | SeaSpine Orthopedics Corporation | 07/01/2026SE |
| K253151 | Fule Interbody Fusion Cage SystemMAX · Traditional | Beijing Fule Science & Technology Development… | 06/15/2026SE |
| K261159 | Exceed® Biplanar Expandable Interbody SystemMAX · Traditional | Spine Wave, Inc. | 05/29/2026SE |
| K253894 | BMD Titanium Spinal Fusion SystemMAX · Traditional | Global Biomedica s.r.o. | 05/28/2026SE |
| K260506 | Ventana® P/T Lumbar Interbody SystemMAX · Traditional | Spinal Elements, Inc. | 05/15/2026SE |
| K260837 | VersaLift Expandable SystemMAX · Traditional | Life Spine, Inc. | 05/12/2026SE |
More from Life Spine, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K231098 | LineSider® Spinal SystemNKB · Traditional | 08/07/2023SE |
| K213355 | Toro-L Interbody Fusion SystemMAX · Traditional | 03/25/2022SE |
| K220453 | FlareHawk Interbody Fusion SystemMAX · Special | 03/24/2022SE |
| K212088 | Integrity Implants Navigated InstrumentsOLO · Traditional | 12/23/2021SE |
| K203038 | Toro-L Interbody Fusion SystemMAX · Traditional | 03/26/2021SE |
| K203367 | LineSider Spinal SystemNKB · Special | 12/03/2020SE |
| K201367 | FlareHawk TiHawk9 Interbody Fusion SystemMAX · Traditional | 09/23/2020SE |
| K190360 | LineSider Spinal SystemNKB · Traditional | 06/21/2019SE |
| K183184 | FlareHawk Interbody Fusion SystemMAX · Traditional | 04/03/2019SE |
| K182114 | FlareHawk Interbody Fusion SystemMAX · Traditional | 01/07/2019SE |
Questions and answers
When was FlareHawk Interbody Fusion System cleared by the FDA?
FlareHawk Interbody Fusion System (K202198) received a 510(k) decision of Substantially Equivalent on November 3, 2020, 90 days after the submission was received.
What is the product code of K202198?
The FDA product code is MAX – Intervertebral Fusion Device With Bone Graft, Lumbar, a Class II (moderate risk) device regulated under 21 CFR 888.3080.