The following data is part of a premarket notification filed by Stockert Gmbh with the FDA for Stockert Neuro N50, Model12267.
| Device ID | K070336 |
| 510k Number | K070336 |
| Device Name: | STOCKERT NEURO N50, MODEL12267 |
| Classification | Generator, Lesion, Radiofrequency |
| Applicant | STOCKERT GMBH BOETZINGER STRASSE 72 Freiburg, B-w, DE D-79111 |
| Contact | Dominika Schuler |
| Correspondent | Dominika Schuler STOCKERT GMBH BOETZINGER STRASSE 72 Freiburg, B-w, DE D-79111 |
| Product Code | GXD |
| CFR Regulation Number | 882.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-02-05 |
| Decision Date | 2007-06-14 |
| Summary: | summary |