ACTIVATOR II

Manipulator, Plunger-like Joint

ACTIVATOR METHODS, INC.

The following data is part of a premarket notification filed by Activator Methods, Inc. with the FDA for Activator Ii.

Pre-market Notification Details

• Device ID: K973506
• 510k Number: K973506
• Device Name: ACTIVATOR II
• Classification: Manipulator, Plunger-like Joint
• Applicant: ACTIVATOR METHODS, INC. 3714 EAST INDIAN SCHOOL RD. Phoenix, AZ 85018
• Contact: Arlan W Fuhr
• Correspondent: Arlan W Fuhr; ACTIVATOR METHODS, INC. 3714 EAST INDIAN SCHOOL RD. Phoenix, AZ 85018
• Product Code: LXM
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1997-09-16
• Decision Date: 1998-01-27
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00850021303044	K973506	000
00850021303020	K973506	000