The following data is part of a premarket notification filed by Neoss Surgery Sl with the FDA for Stern Fix Sternal Stabilization System.
Device ID | K211613 |
510k Number | K211613 |
Device Name: | Stern Fix Sternal Stabilization System |
Classification | Cerclage, Fixation |
Applicant | Neoss Surgery SL Parc Technologic Del Valles Barcelona, ES 08290 |
Contact | Eduard Garcia Puig |
Correspondent | Cherita James M Squared Associates, Inc 127 West 30th Street, 9th Floor New York, NY 10001 |
Product Code | JDQ |
CFR Regulation Number | 888.3010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-05-26 |
Decision Date | 2022-01-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STERN FIX STERNAL STABILIZATION SYSTEM 79309999 not registered Live/Pending |
NEOS SURGERY, S.L. 2021-01-12 |