The following data is part of a premarket notification filed by Biomet Sports Medicine, Inc. with the FDA for Subtalar Implant.
Device ID | K071498 |
510k Number | K071498 |
Device Name: | SUBTALAR IMPLANT |
Classification | Screw, Fixation, Bone |
Applicant | BIOMET SPORTS MEDICINE, INC. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Elizabeth Wray |
Correspondent | Elizabeth Wray BIOMET SPORTS MEDICINE, INC. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-05-31 |
Decision Date | 2007-07-31 |
Summary: | summary |