Cleared Special

K142095 - RENOVIS S134 ANTERIOR LUMBAR INTERBODY ...

K142095 is the FDA 510(k) clearance for RENOVIS S134 ANTERIOR LUMBAR INTERBODY ... by Renovis Surgical Technologies, Inc.. It is a Class 2 Orthopedic device (product code OVD) cleared through the Special 510(k) pathway after a 75-day FDA review.

K142095 · Renovis Surgical Technologies, Inc. · Orthopedic device
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Oct 2014
Decision
75d
Days
Class 2
Risk

K142095 is an FDA 510(k) clearance for the RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM. Classified as Intervertebral Fusion Device With Integrated Fixation, Lumbar (product code OVD), Class II - Special Controls.

Submitted by Renovis Surgical Technologies, Inc. (Ashland, US). The FDA issued a Cleared decision on October 15, 2014 after a review of 75 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3080 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Renovis Surgical Technologies, Inc. devices

Submission Details

510(k) Number K142095 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 2014
Decision Date October 15, 2014
Days to Decision 75 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
47d faster than avg
Panel avg: 122d · This submission: 75d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Lumbar Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft With Or Without Supplemental Fixation.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

All 148
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