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 |