VSP SYSTEM

Driver, Wire, And Bone Drill, Manual

MEDICAL MODELING INC

The following data is part of a premarket notification filed by Medical Modeling Inc with the FDA for Vsp System.

Pre-market Notification Details

• Device ID: K120956
• 510k Number: K120956
• Device Name: VSP SYSTEM
• Classification: Driver, Wire, And Bone Drill, Manual
• Applicant: MEDICAL MODELING INC 555 THIRTEENTH STREET, NW Washington, DC 20004
• Contact: Jonathan S Kahan
• Correspondent: Jonathan S Kahan; MEDICAL MODELING INC 555 THIRTEENTH STREET, NW Washington, DC 20004
• Product Code: DZJ
• CFR Regulation Number: 872.4120 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2012-03-30
• Decision Date: 2012-12-12
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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