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 |