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 |