The following data is part of a premarket notification filed by Radionics, Inc. with the FDA for Modification To Optical Tracking System (ots).
| Device ID | K001431 |
| 510k Number | K001431 |
| Device Name: | MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS) |
| Classification | Neurological Stereotaxic Instrument |
| Applicant | RADIONICS, INC. 22 TERRY AVE. Burlington, MA 01803 -2516 |
| Contact | Kevin J O'connell |
| Correspondent | Kevin J O'connell RADIONICS, INC. 22 TERRY AVE. Burlington, MA 01803 -2516 |
| Product Code | HAW |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-05-08 |
| Decision Date | 2000-05-17 |