Cleared Traditional

K150695 - Modpod

K150695 is an FDA 510(k) clearance for Modpod, manufactured by Hollywog, LLC. The device is a Class 2 Physical Medicine device with product code ITH cleared through the Traditional 510(k) pathway after a 148-day FDA review.

K150695 · Hollywog, LLC · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2015
Decision
148d
Days
Class 2
Risk

K150695 is an FDA 510(k) clearance for the Modpod. Classified as Equipment, Traction, Powered (product code ITH), Class II - Special Controls.

Submitted by Hollywog, LLC (Chattanooga, US). The FDA issued a Cleared decision on August 13, 2015 after a review of 148 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5900 - the FDA physical medicine device 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 Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Hollywog, LLC devices

FDA 510(k) Submission Details - K150695

510(k) Number K150695 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 2015
Decision Date August 13, 2015
Days to Decision 148 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
33d slower than avg
Panel avg: 115d · This submission: 148d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ITH Device Classification - Class 2, Special Controls

Product Code ITH Equipment, Traction, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5900
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - ITH Equipment, Traction, Powered

All 11
Devices cleared under the same product code (ITH) and FDA review panel - the closest regulatory comparables to K150695.
DRX9000C-SL Cervical Spinal Decompression System
K243366 · Excite Medical of Tampa Bay, LLC · Jun 2025
Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-Trac
K214037 · Ergo-Flex Technologies, LLC · Feb 2024
c1Trac
K222912 · Zimmer Medizinsysteme GmbH · May 2023
EVERYWAY TRACTION UNIT, MODEL EVER-TRAC ET-800
K112074 · Everyway Medical Instruments Co.,Ltd · Feb 2012
MTD 4000
K091540 · Mettler Electronics Corp. · Oct 2009
DYNATRON 900
K993919 · Dynatronics Corp. · Jan 2000