The following data is part of a premarket notification filed by Ulrich Gmbh & Co. Kg with the FDA for Neon3.
Device ID | K150650 |
510k Number | K150650 |
Device Name: | Neon3 |
Classification | Posterior Cervical Screw System |
Applicant | ULRICH GMBH & CO. KG BUCHBRUNNENWEG 12 Ulm, DE 89081 |
Contact | Christoph Ulrich |
Correspondent | Hans Stover ulrich Medical USA 18221 Edison Avenue Chesterfield, MO 63005 |
Product Code | NKG |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-12 |
Decision Date | 2015-09-24 |
Summary: | summary |