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 |