The following data is part of a premarket notification filed by Renovo, Inc. with the FDA for Reprocessed Depuy Mitek Ablation Wand.
Device ID | K173740 |
510k Number | K173740 |
Device Name: | Reprocessed DePuy Mitek Ablation Wand |
Classification | Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
Applicant | ReNovo, Inc. 340 SW Columbia St. Bend, OR 97702 |
Contact | Mark K. Wells |
Correspondent | Robert V. Packard Medical Device Academy, Inc. 345 Lincoln Hill Rd. Shrewsbury, VT 05738 |
Product Code | NUJ |
Subsequent Product Code | GEI |
Subsequent Product Code | HRX |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-07 |
Decision Date | 2018-03-19 |
Summary: | summary |