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 |