The following data is part of a premarket notification filed by Biopro, Inc. with the FDA for Modification To Hbs Headless Bone Screw.
| Device ID | K101030 |
| 510k Number | K101030 |
| Device Name: | MODIFICATION TO HBS HEADLESS BONE SCREW |
| Classification | Screw, Fixation, Bone |
| Applicant | BIOPRO, INC. 2929 LAPEER ROAD Port Huron, MI 48060 |
| Contact | David Mrak |
| Correspondent | David Mrak BIOPRO, INC. 2929 LAPEER ROAD Port Huron, MI 48060 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-04-13 |
| Decision Date | 2010-06-03 |
| Summary: | summary |