The following data is part of a premarket notification filed by Biopro, Inc. with the FDA for Biopro Go-ez Screw.
| Device ID | K081149 |
| 510k Number | K081149 |
| Device Name: | BIOPRO GO-EZ SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | BIOPRO, INC. 17 SEVENTEENTH ST. Port Huron, MI 48060 |
| Contact | David Mrak |
| Correspondent | David Mrak BIOPRO, INC. 17 SEVENTEENTH ST. Port Huron, MI 48060 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-04-22 |
| Decision Date | 2008-08-05 |