The following data is part of a premarket notification filed by Ulrich Gmbh & Co. Kg with the FDA for Neon System.
Device ID | K113346 |
510k Number | K113346 |
Device Name: | NEON SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | ULRICH GMBH & CO. KG 612 TRADE CENTER BLVD Chesterfield, MO 63005 |
Contact | Hans Stover |
Correspondent | Hans Stover ULRICH GMBH & CO. KG 612 TRADE CENTER BLVD Chesterfield, MO 63005 |
Product Code | KWP |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-11-14 |
Decision Date | 2012-02-28 |
Summary: | summary |