The following data is part of a premarket notification filed by Epic Extremity, Llc with the FDA for Epic Extremity Cannulated Screw System.
Device ID | K153333 |
510k Number | K153333 |
Device Name: | Epic Extremity Cannulated Screw System |
Classification | Screw, Fixation, Bone |
Applicant | Epic Extremity, LLC 120 Marguerite Dr, Ste 301 Cranberry Twp, PA 16066 |
Contact | Dan Schwartzbauer |
Correspondent | Lee Strnad Intrepid Orthopedics, LLC 3046 Brecksville Road, Suite 4 Richfield, OH 44286 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-11-19 |
Decision Date | 2016-01-19 |
Summary: | summary |