The following data is part of a premarket notification filed by Iconn Orthopedics, Llc with the FDA for Iconn Answer Suture Anchor.
Device ID | K132724 |
510k Number | K132724 |
Device Name: | ICONN ANSWER SUTURE ANCHOR |
Classification | Fastener, Fixation, Nondegradable, Soft Tissue |
Applicant | ICONN ORTHOPEDICS, LLC 400 UNION HILL DR SUITE 150 Birmingham, AL 35209 |
Contact | Whitt Israel |
Correspondent | Whitt Israel ICONN ORTHOPEDICS, LLC 400 UNION HILL DR SUITE 150 Birmingham, AL 35209 |
Product Code | MBI |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-08-30 |
Decision Date | 2014-04-17 |