The following data is part of a premarket notification filed by Techmedica, Inc. with the FDA for Techmedica Standard Bipolar System.
| Device ID | K925420 |
| 510k Number | K925420 |
| Device Name: | TECHMEDICA STANDARD BIPOLAR SYSTEM |
| Classification | Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented |
| Applicant | TECHMEDICA, INC. 3760 CALLE TECATE Camarillo, CA 93012 |
| Contact | Dave Samson |
| Correspondent | Dave Samson TECHMEDICA, INC. 3760 CALLE TECATE Camarillo, CA 93012 |
| Product Code | KWY |
| CFR Regulation Number | 888.3390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-27 |
| Decision Date | 1993-09-28 |