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 |