The following data is part of a premarket notification filed by Osteomed Llc with the FDA for Osteomed Extremifix Mini & Small Cannulated Screw System.
Device ID | K202680 |
510k Number | K202680 |
Device Name: | OsteoMed ExtremiFix Mini & Small Cannulated Screw System |
Classification | Screw, Fixation, Bone |
Applicant | OsteoMed LLC 3885 Arapaho Road Addison, TX 75001 |
Contact | Andrew "drew" Johnson |
Correspondent | Andrew "drew" Johnson OsteoMed LLC 3885 Arapaho Road Addison, TX 75001 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-09-15 |
Decision Date | 2020-10-15 |