The following data is part of a premarket notification filed by Nakanishi, Inc. with the FDA for Primado2 Total Surgical System.
| Device ID | K132264 |
| 510k Number | K132264 |
| Device Name: | PRIMADO2 TOTAL SURGICAL SYSTEM |
| Classification | Motor, Drill, Electric |
| Applicant | NAKANISHI, INC. 1201 RICHARDSON DRIVE SUITE 280 Richardson, TX 75080 |
| Contact | Diane Rutherford |
| Correspondent | Diane Rutherford NAKANISHI, INC. 1201 RICHARDSON DRIVE SUITE 280 Richardson, TX 75080 |
| Product Code | HBC |
| Subsequent Product Code | ERL |
| Subsequent Product Code | HBE |
| Subsequent Product Code | HWE |
| CFR Regulation Number | 882.4360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-07-22 |
| Decision Date | 2013-12-17 |
| Summary: | summary |