Hummingbird(Tm) Tympanostomy Tube System (TTS)

FDA 510(k) K142282 · Preceptis Medical

Substantially Equivalent

510(k) numberK142282

Submission

Device name
Hummingbird(Tm) Tympanostomy Tube System (TTS)
Applicant
Preceptis Medical
Plymouth, MN, US
Received
August 15, 2014
Decision date
April 23, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ETD – Tube, Tympanostomy
Device class
Class II (moderate risk)
Regulation
21 CFR 874.3880
Specialty
Ear, Nose, Throat
Implant
Yes

Other 510(k)s with product code ETD

510(k)DeviceApplicantDecision
K252436Tula Tympanostomy Tube Delivery DeviceETD · Traditional Tusker Medical, Inc.04/23/2026SE
K250256Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube…ETD · Traditional Aventamed Dac04/28/2025SE
K232702Solo+ Tympanostomy Tube Device (TTD)ETD · Traditional Aventamed Dac05/20/2024SE
K233658Biowy Tym Tube (TT)ETD · Traditional Biowy Corporation02/16/2024SE
K232059Tympanostomy TubesETD · Traditional Grace Medical, Inc.11/24/2023SE
K221254Hummingbird Tympanostomy Tube SystemETD · Traditional Preceptis Medical, Inc.07/27/2022SE
K200952Hummingbird Tympanostomy Tube SystemETD · Traditional Preceptis Medical, Inc.06/05/2020SE
K171239TULA Tube Delivery SystemETD · Special Tusker Medical06/28/2017SE
K151830Hummingbird Tympanostomy TubeETD · Traditional Preceptis Medical09/21/2015SE
K151067Ventilation (Tympanostomy) TubesETD · Traditional Medtronic Xomed, Inc.07/22/2015SE

More from Medtronic Xomed, Inc.

510(k)DeviceDecision
K221254Hummingbird Tympanostomy Tube SystemETD · Traditional 07/27/2022SE
K200952Hummingbird Tympanostomy Tube SystemETD · Traditional 06/05/2020SE
K151830Hummingbird Tympanostomy TubeETD · Traditional 09/21/2015SE
K133921Preceptis Tympanostomy Tube InserterETD · Traditional 08/22/2014SE

Questions and answers

When was Hummingbird(Tm) Tympanostomy Tube System (TTS) cleared by the FDA?

Hummingbird(Tm) Tympanostomy Tube System (TTS) (K142282) received a 510(k) decision of Substantially Equivalent on April 23, 2015, 251 days after the submission was received.

What is the product code of K142282?

The FDA product code is ETD – Tube, Tympanostomy, a Class II (moderate risk) device regulated under 21 CFR 874.3880.