The following data is part of a premarket notification filed by Oco Biomedical with the FDA for Tsi; Eri.
Device ID | K090174 |
510k Number | K090174 |
Device Name: | TSI; ERI |
Classification | Implant, Endosseous, Root-form |
Applicant | OCO BIOMEDICAL 8500 WASHINGTON ST. NE SUITE A-1 Albuquerque, NM 87113 |
Contact | Jack Bloom |
Correspondent | Jack Bloom OCO BIOMEDICAL 8500 WASHINGTON ST. NE SUITE A-1 Albuquerque, NM 87113 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-01-23 |
Decision Date | 2009-09-14 |
Summary: | summary |