The following data is part of a premarket notification filed by Midwest Implant Sales, Inc. with the FDA for Midwest Implant Hexed 3.75mm Self Tapping Implant.
Device ID | K914042 |
510k Number | K914042 |
Device Name: | MIDWEST IMPLANT HEXED 3.75MM SELF TAPPING IMPLANT |
Classification | Implant, Endosseous, Root-form |
Applicant | MIDWEST IMPLANT SALES, INC. P.O. BOX 681038 Schaumburg, IL 60168 |
Contact | John T Corsten |
Correspondent | John T Corsten MIDWEST IMPLANT SALES, INC. P.O. BOX 681038 Schaumburg, IL 60168 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-09-10 |
Decision Date | 1991-12-09 |