The following data is part of a premarket notification filed by Levita Magnetics International Corp. with the FDA for Magnetic Surgical System.
Device ID | K171429 |
510k Number | K171429 |
Device Name: | Magnetic Surgical System |
Classification | Magnetic Surgical System |
Applicant | Levita Magnetics International Corp. 1730 S. Amphlett Blvd, Suite 240 San Mateo, CA 94402 |
Contact | Alberto Rodrigues-navarro |
Correspondent | Cindy Domecus Domescus Consulting Services LLc 1171 Barroilhet Drive Hillsborough, CA 94010 |
Product Code | PNL |
CFR Regulation Number | 878.4815 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-15 |
Decision Date | 2017-06-06 |
Summary: | summary |