The following data is part of a premarket notification filed by Danlin Products, Inc. with the FDA for B.a.s.i.c. Dental Implant System.
| Device ID | K960868 |
| 510k Number | K960868 |
| Device Name: | B.A.S.I.C. DENTAL IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | DANLIN PRODUCTS, INC. 3321 COLUMBIA, N.E. Albuquerque, NM 87107 -2001 |
| Contact | Dan Blacklock |
| Correspondent | Dan Blacklock DANLIN PRODUCTS, INC. 3321 COLUMBIA, N.E. Albuquerque, NM 87107 -2001 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-04 |
| Decision Date | 1996-11-14 |