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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact