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 |