The following data is part of a premarket notification filed by Epic Extremity, Llc with the FDA for Epic Extremity Fusion Plate System.
Device ID | K182991 |
510k Number | K182991 |
Device Name: | EPIC Extremity Fusion Plate System |
Classification | Plate, Fixation, Bone |
Applicant | EPIC Extremity, LLC 120 Marguerite Drive, Suite 301 Cranberry Twp, PA 16066 |
Contact | Dan Schwartzbauer |
Correspondent | Randy Schlemmer EPIC Extremity, LLC 120 Marguerite Drive, Suite 301 Cranberry Twp, PA 16066 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-10-29 |
Decision Date | 2019-02-13 |
Summary: | summary |