Life Spine Metatarsal Hemi Implant
FDA 510(k) K161279 · Life Spine, Inc.
510(k) numberK161279
Submission
- Device name
- Life Spine Metatarsal Hemi Implant
- Applicant
- Life Spine, Inc.
Huntley, IL, US - Received
- May 6, 2016
- Decision date
- February 1, 2017
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KWD – Prosthesis, Toe, Hemi-, Phalangeal
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3730
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KWD
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K250074 | HYALEX® MTP Hemiarthroplasty ImplantKWD · Traditional | Hyalex Orthopaedics, Inc. | 04/03/2026SE |
| K240268 | Accu-Joint Hemi ImplantKWD · Special | Accufix Surgical, Inc. | 02/29/2024SE |
| K221220 | Montross Extremity Medical Hemi Implant SystemKWD · Traditional | Montross Extremity Medical | 04/19/2023SE |
| K222964 | BioPoly Lesser Toe Hemiarthroplasty ImplantKWD · Traditional | BioPoly, LLC | 11/22/2022SE |
| K201393 | restor3d MTP ImplantKWD · Traditional | Restor3D, Inc. | 05/25/2022SE |
| K203634 | BioPoly Great Toe Hemiarthroplasty ImplantKWD · Traditional | BioPoly, LLC | 02/02/2021SE |
| K200951 | Accu-Joint Hemi ImplantKWD · Traditional | Accufix Surgical, Inc. | 12/08/2020SE |
| K190261 | BOSS Toe Fixation SystemKWD · Traditional | Arthrosurface, Inc. | 08/14/2019SE |
| K190543 | Cannulated Hemi ImplantKWD · Traditional | Vilex IN Tennessee, Inc. | 05/31/2019SE |
| K152454 | HemiCAP MTP Resurfacing Hemi-Arthroplasty SystemKWD · Special | Arthrosurface, Inc. | 04/11/2016SE |
More from Arthrosurface, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K261430 | TruLift Expandable SystemMAX · Traditional | 07/28/2026SE |
| K260571 | SIMPACT Sacroiliac Joint Fixation System GX Navigation InstrumentsOLO · Traditional | 06/02/2026SE |
| K260837 | VersaLift Expandable SystemMAX · Traditional | 05/12/2026SE |
| K254274 | ARx® SAI Implant SystemNKB · Traditional | 04/16/2026SE |
| K253748 | Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer SystemMAX · Traditional | 01/23/2026SE |
| K251502 | TruLift® Lateral Expandable Spacer & Lateral Buttress Plate SystemMAX · Traditional | 07/07/2025SE |
| K250373 | ProLift Expandable Spacer SystemMAX · Traditional | 04/09/2025SE |
| K243668 | ProLift Pivot Expandable Spacer SystemMAX · Traditional | 01/23/2025SE |
| K243369 | Cervical Plating SystemKWQ · Traditional | 12/11/2024SE |
| K242826 | ProLift Wedge Expandable Spacer SystemMAX · Traditional | 10/08/2024SE |
Questions and answers
When was Life Spine Metatarsal Hemi Implant cleared by the FDA?
Life Spine Metatarsal Hemi Implant (K161279) received a 510(k) decision of Substantially Equivalent on February 1, 2017, 271 days after the submission was received.
What is the product code of K161279?
The FDA product code is KWD – Prosthesis, Toe, Hemi-, Phalangeal, a Class II (moderate risk) device regulated under 21 CFR 888.3730.