The following data is part of a premarket notification filed by X-nav Technologies, Llc with the FDA for X-guide Surgical Navigation System.
Device ID | K150222 |
510k Number | K150222 |
Device Name: | X-Guide Surgical Navigation System |
Classification | Dental Stereotaxic Instrument |
Applicant | X-Nav Technologies, LLC 1555 Bustard Road, Suite 75 Lansdale, PA 19446 |
Contact | Fred Cowdery |
Correspondent | Fred Cowdery X-Nav Technologies, LLC 1555 Bustard Road, Suite 75 Lansdale, PA 19446 |
Product Code | PLV |
CFR Regulation Number | 872.4120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-01-30 |
Decision Date | 2015-10-08 |
Summary: | summary |