The following data is part of a premarket notification filed by Lifecore Biomedical, Inc. with the FDA for Capset Calcium Sulfate Bone Graft Plaster.
| Device ID | K943186 |
| 510k Number | K943186 |
| Device Name: | CAPSET CALCIUM SULFATE BONE GRAFT PLASTER |
| Classification | Bone Grafting Material, Synthetic |
| Applicant | LIFECORE BIOMEDICAL, INC. 3515 LYMAN BLVD. Chaska, MN 55318 |
| Contact | Lynn Cuperus |
| Correspondent | Lynn Cuperus LIFECORE BIOMEDICAL, INC. 3515 LYMAN BLVD. Chaska, MN 55318 |
| Product Code | LYC |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-07-05 |
| Decision Date | 1995-04-10 |