The following data is part of a premarket notification filed by Wieland Dental + Technik Gmbh & Co. Kg with the FDA for Xawex G 100.
Device ID | K050903 |
510k Number | K050903 |
Device Name: | XAWEX G 100 |
Classification | Powder, Porcelain |
Applicant | WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRASSE 13 Pforzheim, DE 75179 |
Contact | Gerhard Polzer |
Correspondent | Gerhard Polzer WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRASSE 13 Pforzheim, DE 75179 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-04-11 |
Decision Date | 2005-06-23 |
Summary: | summary |