The following data is part of a premarket notification filed by Implant Integration Systems, Inc. with the FDA for Implant Integration Systems Drills And Taps.
Device ID | K962394 |
510k Number | K962394 |
Device Name: | IMPLANT INTEGRATION SYSTEMS DRILLS AND TAPS |
Classification | Implant, Endosseous, Root-form |
Applicant | IMPLANT INTEGRATION SYSTEMS, INC. 6161 CLARK RD., STE. 8 Paradise, CA 95969 |
Contact | Cory D Hanosh |
Correspondent | Cory D Hanosh IMPLANT INTEGRATION SYSTEMS, INC. 6161 CLARK RD., STE. 8 Paradise, CA 95969 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-06-20 |
Decision Date | 1996-10-11 |
Summary: | summary |