The following data is part of a premarket notification filed by Medtronic Xomed, Inc. with the FDA for Ventilation (tympanostomy) Tubes.
| Device ID | K151067 |
| 510k Number | K151067 |
| Device Name: | Ventilation (Tympanostomy) Tubes |
| Classification | Tube, Tympanostomy |
| Applicant | Medtronic Xomed, Inc. 6743 Southpoint Drive North Jacksonville, FL 32216 |
| Contact | Michelle Hughes |
| Correspondent | Michelle Hughes Medtronic Xomed, Inc. 6743 Southpoint Drive North Jacksonville, FL 32216 |
| Product Code | ETD |
| CFR Regulation Number | 874.3880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-04-21 |
| Decision Date | 2015-07-22 |
| Summary: | summary |