510(k) K160074
- Device
- Rampart D Lumbar Interbody Fusion Device
- Applicant
- Spineology Inc.
- 510(k) number
- K160074
- Product code
- MAX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2016-10-18
- Date received
- 2016-01-14
- Regulation
- 888.3080
- Classification name
- Intervertebral Fusion Device With Bone Graft, Lumbar
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- Karen Roche
- Address
- 7800 Third St. N., Suite 600 Saint Paul MN US 55128 55128
FDA Registration Numbers#
- 3010057495
- 3010370500
- 3009957608
- 3010646402
- 3031284747
- 3007200272
- 9615766
- 3006791286
- 1528646
- 3042226236
- 1834379
- 3015179588
- 3004976965
- 3025603301
- 3000203391
- 3015426608
- 3005641619
- 3011181154
- 3015398319
- 3017565094
- 3007887127
- 3009826895
- 3012764194
- 3006082533
- 3009882675
- 1833986
- 3010120135
- 3011648620
- 2530808
- 3005751028
- 3012028003
- 3011127597
- 3012994232
- 3021588295
- 3009129735
- 9611813
- 3019356409
- 3022295665
- 3009404219
- 3018210489
- 3009973505
- 3014315669
- 3016460869
- 3009049161
- 3007289746
- 3007345964
- 1424263
- 3015151147
- 3007766601
- 3008102042
- 3009132077
- 3009988302
- 3021945817
- 9615128
- 3014252644
- 3004774118
- 2648623
- 3033739814
- 3013422238
- 3036756245
- 3016438694
- 1643817
- 3031240334
- 3008285983
- 3016244279
- 1047843
- 3004941535
- 1319660
- 3006404071
- 1526711
- 3004024955
- 8010273
- 3013546462
- 3009998573
- 3006639944
- 3004788213
- 1057425
- 3036503733
- 3009165919
- 3017048829
Source Documents#
Other 510(k) Records For Product Code MAX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K261049 | SCALA® TL | Spineart SA | 2026-08-20 |
| K261430 | TruLift Expandable System | Life Spine, Inc. | 2026-07-28 |
| K253011 | Catalyft PL Expandable Interbody System | Medtronic Sofamor Danek USA, Inc. | 2026-07-17 |
| K261020 | Symmetrix™ L Spinal System | Medtronic Sofamor Danek USA, Inc. | 2026-07-14 |
| K253420 | Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody Sy | SeaSpine Orthopedics Corporation | 2026-07-01 |
| K253151 | Fule Interbody Fusion Cage System | Beijing Fule Science & Technology Development Co., Ltd. | 2026-06-15 |
| K261159 | Exceed® Biplanar Expandable Interbody System | Spine Wave, Inc. | 2026-05-29 |
| K253894 | BMD Titanium Spinal Fusion System | Global Biomedica s.r.o. | 2026-05-28 |
| K260506 | Ventana® P/T Lumbar Interbody System | Spinal Elements, Inc. | 2026-05-15 |
| K260837 | VersaLift Expandable System | Life Spine, Inc. | 2026-05-12 |
| K260385 | aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating system | Carlsmed, Inc. | 2026-05-09 |
| K261067 | BEE PLIF Cage | NGMedical GmbH | 2026-04-30 |
| K254017 | SWINGO-3D Lumbar Cage System | Implanet | 2026-02-26 |
| K253583 | LUX Expandable Lumbar Interbody System | Xenix Medical | 2026-02-23 |
| K250773 | Luna® Ti Interbody Fusion System | Spinal Elements, Inc. | 2026-02-04 |
Legacy Summary#
summary
FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases