The following data is part of a premarket notification filed by Lifecore Biomedical, Inc. with the FDA for Lifecore Conical Abutment.
| Device ID | K965135 |
| 510k Number | K965135 |
| Device Name: | LIFECORE CONICAL ABUTMENT |
| Classification | Implant, Endosseous, Root-form |
| Applicant | LIFECORE BIOMEDICAL, INC. 3515 LYMAN BLVD. Chaska, MN 55318 |
| Contact | Donna Bahls |
| Correspondent | Donna Bahls LIFECORE BIOMEDICAL, INC. 3515 LYMAN BLVD. Chaska, MN 55318 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-12-23 |
| Decision Date | 1997-02-25 |
| Summary: | summary |