The following data is part of a premarket notification filed by Techmedica, Inc. with the FDA for Techmedica Mp System.
| Device ID | K882922 |
| 510k Number | K882922 |
| Device Name: | TECHMEDICA MP SYSTEM |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
| Applicant | TECHMEDICA, INC. 1380 FLYNN RD. Camarillo, CA 93010 |
| Contact | Rick A Buss |
| Correspondent | Rick A Buss TECHMEDICA, INC. 1380 FLYNN RD. Camarillo, CA 93010 |
| Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-13 |
| Decision Date | 1988-09-22 |