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 |