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 |