The following data is part of a premarket notification filed by Implant Innovations, Inc. with the FDA for 3i Single Use, Disposable Drills,taps,burs, Etc..
Device ID | K962014 |
510k Number | K962014 |
Device Name: | 3I SINGLE USE, DISPOSABLE DRILLS,TAPS,BURS, ETC. |
Classification | Implant, Endosseous, Root-form |
Applicant | IMPLANT INNOVATIONS, INC. 3071 CONTINENTAL DR. West Palm Beach, FL 33407 |
Contact | William G Conety |
Correspondent | William G Conety IMPLANT INNOVATIONS, INC. 3071 CONTINENTAL DR. West Palm Beach, FL 33407 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-05-23 |
Decision Date | 1996-10-18 |
Summary: | summary |