The following data is part of a premarket notification filed by Brainlab, Ag with the FDA for Modification To Vectorvision Trauma.
| Device ID | K062358 |
| 510k Number | K062358 |
| Device Name: | MODIFICATION TO VECTORVISION TRAUMA |
| Classification | Neurological Stereotaxic Instrument |
| Applicant | BRAINLAB, AG KAPELLENSTR. 12 Feldkirchen, DE 85622 |
| Contact | Rainer Birkenbach |
| Correspondent | Rainer Birkenbach BRAINLAB, AG KAPELLENSTR. 12 Feldkirchen, DE 85622 |
| Product Code | HAW |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-14 |
| Decision Date | 2007-01-17 |
| Summary: | summary |