Modpod

Equipment, Traction, Powered

HOLLYWOG, LLC

The following data is part of a premarket notification filed by Hollywog, Llc with the FDA for Modpod.

Pre-market Notification Details

• Device ID: K150695
• 510k Number: K150695
• Device Name: Modpod
• Classification: Equipment, Traction, Powered
• Applicant: HOLLYWOG, LLC 2830 AMMICOLA HIGHWAY Chattanooga, TN 37377
• Contact: Michael Treas
• Correspondent: Michael Treas; HOLLYWOG, LLC 2830 AMMICOLA HIGHWAY Chattanooga, TN 37377
• Product Code: ITH
• CFR Regulation Number: 890.5900 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2015-03-18
• Decision Date: 2015-08-13
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10853096004158	K150695	000