The following data is part of a premarket notification filed by Merete Medical Gmbh with the FDA for Metafix Ls Locking Screws, Merete Cannulated Pcs, Merete Cs Cortical Screws, Merete Cannulated Hcs, Duothread Scarf Screws And Twistcut Snap-off Screws.
Device ID | K152187 |
510k Number | K152187 |
Device Name: | MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws, Merete Cannulated HCS, DuoThread Scarf Screws And TwistCut Snap-Off Screws |
Classification | Screw, Fixation, Bone |
Applicant | MERETE MEDICAL GMBH ALT-LANKWITZ 102 Berlin, DE 12247 |
Contact | Emmanuel Anapliotis |
Correspondent | Matthias Mollmann MERETE MEDICAL, INC 4 CROTTY LANE-SUITE 118, NEW YORK INTERNATIONAL PLAZA New Windsor, NY 12553 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-08-05 |
Decision Date | 2016-02-12 |
Summary: | summary |