The following data is part of a premarket notification filed by Medtronic Xomed, Inc. with the FDA for Stimulus - Dissection Instruments.
| Device ID | K014165 |
| 510k Number | K014165 |
| Device Name: | STIMULUS - DISSECTION INSTRUMENTS |
| Classification | Stimulator, Nerve |
| Applicant | MEDTRONIC XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 |
| Contact | Martin D Sargent |
| Correspondent | Martin D Sargent MEDTRONIC XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 |
| Product Code | ETN |
| CFR Regulation Number | 874.1820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-12-19 |
| Decision Date | 2002-01-22 |
| Summary: | summary |