MT-2

Implant, Endosseous, Root-form

THE EMERGING TECHNOLOGIES GROUP

The following data is part of a premarket notification filed by The Emerging Technologies Group with the FDA for Mt-2.

Pre-market Notification Details

• Device ID: K961384
• 510k Number: K961384
• Device Name: MT-2
• Classification: Implant, Endosseous, Root-form
• Applicant: THE EMERGING TECHNOLOGIES GROUP 824 U.S. HWY. 1, SUITE 370 North Palm Beach, FL 33408
• Contact: Jack T Krauser
• Correspondent: Jack T Krauser; THE EMERGING TECHNOLOGIES GROUP 824 U.S. HWY. 1, SUITE 370 North Palm Beach, FL 33408
• Product Code: DZE
• CFR Regulation Number: 872.3640 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-03-19
• Decision Date: 1996-09-25
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
D86336730	K961384	000
D86358190	K961384	000
D86358180	K961384	000
D86358170	K961384	000
D86358160	K961384	000
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D86358140	K961384	000
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00198168629031	K961384	000
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D86336930	K961384	000
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D86337030	K961384	000
D86337020	K961384	000
D86337010	K961384	000
D86336780	K961384	000