The following data is part of a premarket notification filed by Merete Medical Gmbh with the FDA for Meretec Cs, Cortical Screws.
Device ID | K130400 |
510k Number | K130400 |
Device Name: | MERETEC CS, CORTICAL SCREWS |
Classification | Screw, Fixation, Bone |
Applicant | MERETE MEDICAL GMBH 102 ALT LANKWITZ Berlin, DE D-12247 |
Contact | Emmanuel Anapliotis |
Correspondent | Emmanuel Anapliotis MERETE MEDICAL GMBH 102 ALT LANKWITZ Berlin, DE D-12247 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-02-19 |
Decision Date | 2013-04-05 |