The following data is part of a premarket notification filed by Steri-oss, Inc. with the FDA for Steri-oss 3.25 Mm Replace(titanium Plasma Sprayed) Dental Implant.
Device ID | K973433 |
510k Number | K973433 |
Device Name: | STERI-OSS 3.25 MM REPLACE(TITANIUM PLASMA SPRAYED) DENTAL IMPLANT |
Classification | Implant, Endosseous, Root-form |
Applicant | STERI-OSS, INC. 22895 EASTPARK DR. Yorba Linda, CA 92887 |
Contact | Jeff Hausheer |
Correspondent | Jeff Hausheer STERI-OSS, INC. 22895 EASTPARK DR. Yorba Linda, CA 92887 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-09-10 |
Decision Date | 1997-12-05 |
Summary: | summary |