The following data is part of a premarket notification filed by Extremity Medical, Llc with the FDA for Omni Foot Plating System.
Device ID | K180808 |
510k Number | K180808 |
Device Name: | Omni Foot Plating System |
Classification | Plate, Fixation, Bone |
Applicant | Extremity Medical, LLC 300 Interpace Parkway, Suite 410 Parsippany, NJ 07054 |
Contact | Brian Smekal |
Correspondent | Brian Smekal Extremity Medical, LLC 300 Interpace Parkway, Suite 410 Parsippany, NJ 07054 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-03-28 |
Decision Date | 2018-05-22 |
Summary: | summary |