The following data is part of a premarket notification filed by Medartis Medizinprodukte Und Forschung Ag with the FDA for Synthacer; Syntricer.
| Device ID | K041177 |
| 510k Number | K041177 |
| Device Name: | SYNTHACER; SYNTRICER |
| Classification | Filler, Bone Void, Calcium Compound |
| Applicant | MEDARTIS MEDIZINPRODUKTE UND FORSCHUNG AG BLUMENSTRASSE 7 Alling, DE 82239 |
| Contact | Hans-peter Wettl |
| Correspondent | Hans-peter Wettl MEDARTIS MEDIZINPRODUKTE UND FORSCHUNG AG BLUMENSTRASSE 7 Alling, DE 82239 |
| Product Code | MQV |
| CFR Regulation Number | 888.3045 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-05-05 |
| Decision Date | 2005-06-23 |
| Summary: | summary |