The following data is part of a premarket notification filed by Corentec Co., Ltd with the FDA for Aegis & Aegis Ii Spinal System.
Device ID | K092076 |
510k Number | K092076 |
Device Name: | AEGIS & AEGIS II SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | CORENTEC CO., LTD 1129 BLOOMFIELD AVE West Caldwell, NJ 07006 |
Contact | Robert Schiff |
Correspondent | Robert Schiff CORENTEC CO., LTD 1129 BLOOMFIELD AVE West Caldwell, NJ 07006 |
Product Code | MNI |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-07-09 |
Decision Date | 2010-04-02 |
Summary: | summary |