FDA 510(k) Applications Submitted by Life Spine, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K220025 |
01/05/2022 |
ARx« Spinal System |
Life Spine, Inc. |
K210061 |
01/11/2021 |
ProLift Lateral HELO Fixated |
Life Spine, Inc. |
K220341 |
02/07/2022 |
ARx Modular Spinal System |
Life Spine, Inc. |
K210549 |
02/25/2021 |
ARx Spinal System |
Life Spine, Inc. |
K191927 |
07/19/2019 |
Hinged Laminoplasty System |
Life Spine, Inc. |
K212520 |
08/10/2021 |
ProLift Micro Expandable Spacer System |
Life Spine, Inc. |
K222628 |
08/31/2022 |
Life Spine ALIF Buttress Plate System |
Life Spine, Inc. |
K212903 |
09/13/2021 |
SIMPACT Sacroiliac Joint Fixation System |
Life Spine, Inc. |
K213417 |
10/20/2021 |
Ghost Spacer System |
Life Spine, Inc. |
K203163 |
10/23/2020 |
ARx Illiac Spinal Screw System |
Life Spine, Inc. |
K223430 |
11/14/2022 |
ProLift Micro Expandable Spacer System |
Life Spine, Inc. |
K203361 |
11/16/2020 |
ProLift Wedge Expandable Spacer System |
Life Spine, Inc. |
K193521 |
12/19/2019 |
Steerable Plateau Ti |
Life Spine, Inc. |
K160066 |
01/13/2016 |
Pro-Link« Stand-Alone Cervical Spacer System |
Life Spine, Inc. |
K180166 |
01/22/2018 |
Life Spine Lumbar Fixation System (SENTRY) |
Life Spine, Inc. |
K150390 |
02/18/2015 |
Nautilus Spinal System |
LIFE SPINE, INC. |
K162685 |
09/26/2016 |
2-Piece Hammertoe Correction System |
Life Spine, Inc. |
K173047 |
09/28/2017 |
The Solstice OCT System |
Life Spine, Inc. |
K153400 |
11/24/2015 |
ProLift Expandable System |
LIFE SPINE, INC. |
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