The following data is part of a premarket notification filed by Merete Medical Gmbh with the FDA for Merete Locking Bone Plate System Iii.
Device ID | K120787 |
510k Number | K120787 |
Device Name: | MERETE LOCKING BONE PLATE SYSTEM III |
Classification | Plate, Fixation, Bone |
Applicant | MERETE MEDICAL GMBH 99 PURCHASE STREET Rye, NY 10580 |
Contact | Donna Coleman |
Correspondent | Donna Coleman MERETE MEDICAL GMBH 99 PURCHASE STREET Rye, NY 10580 |
Product Code | HRS |
Subsequent Product Code | HTY |
Subsequent Product Code | HWC |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-03-15 |
Decision Date | 2012-11-27 |
Summary: | summary |