Cleared Traditional

K131669 - PERIMETER INTERBODY FUSION DEVICE

K131669 is an FDA 510(k) clearance for PERIMETER INTERBODY FUSION DEVICE, manufactured by Medtronic Sofamor Danek USA, Inc.. The device is a Class 2 Orthopedic device with product code MAX cleared through the Traditional 510(k) pathway after a 147-day FDA review.

K131669 · Medtronic Sofamor Danek USA, Inc. · Orthopedic device
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Nov 2013
Decision
147d
Days
Class 2
Risk

K131669 is an FDA 510(k) clearance for the PERIMETER INTERBODY FUSION DEVICE. Classified as Intervertebral Fusion Device With Bone Graft, Lumbar within the MAX classification (a category for intervertebral fusion devices and spinal implants), Class II - Special Controls.

Submitted by Medtronic Sofamor Danek USA, Inc. (Memphis, US). The FDA issued a Cleared decision on November 1, 2013 after a review of 147 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3080 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Medtronic Sofamor Danek USA, Inc. devices

FDA 510(k) Submission Details - K131669

510(k) Number K131669 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 07, 2013
Decision Date November 01, 2013
Days to Decision 147 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
25d slower than avg
Panel avg: 122d · This submission: 147d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MAX Device Classification - Class 2, Special Controls

Product Code MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft.
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 - MAX Intervertebral Fusion Device With Bone Graft, Lumbar

All 849
Devices cleared under the same product code (MAX) and FDA review panel - the closest regulatory comparables to K131669.
CLYDESDALE SPINAL SYSTEM
K132897 · Medtronic Sofamor Danek, Inc. · Dec 2013
K7 LUMBAR SPACERS
K133126 · K7, LLC · Dec 2013
CRESCENT SPINAL SYSTEM
K133216 · Medtronic Sofamor Danek, Inc. · Nov 2013
BIOLIGN ACIF SYSTEMS, BIOLIGN STACC ACIF SYSTEM, BIOLIGN TLIF SYSTEM
K130274 · Elite Surgical Supplies (Pty), Ltd. · Oct 2013
CALIX LUMBAR SPINAL IMPLANT SYSTEM
K131350 · X-Spine Systems, Inc. · Oct 2013
PROW FUSION
K130254 · Nlt Spine, Ltd. · Oct 2013