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 |