SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF

Q: What is the product code of K153783?

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.

FDA 510(k) K153783 · Spinevision S.A.

Substantially Equivalent

510(k) numberK153783

Submission

Device name: SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF
Applicant: Spinevision S.A.
Antony, FR
Received: December 31, 2015
Decision date: May 4, 2016
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

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.

Other 510(k)s with product code MAX

510(k)	Device	Applicant	Decision
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
K160124	LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation SystemMNI · Special	04/04/2016SE
K133575	Spinevision Lumis Cannulated Pedicle Screw Fixation System, Spinevision U.L.I.S. Pedicle…MNH · Traditional	06/30/2014SE
K130302	Spinevision Lumis Cannulated Polyaxial Pedicle Screw Fixation System, Spinevision…MNI · Special	07/30/2013SE
K112607	Spinevision Lumis(Tm) Cannulated Polyaxial Pedicle Screw Fixation System, Spinevision…NKB · Traditional	06/07/2012SE

Questions and answers

When was SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF cleared by the FDA?

SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF (K153783) received a 510(k) decision of Substantially Equivalent on May 4, 2016, 125 days after the submission was received.

What is the product code of K153783?

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.