True Tulip, True M.I.S.
K-Number: K220297 · 2022-09-16
Device Summary
Frequently Asked Questions
What is the True Tulip, True M.I.S.?
True Tulip, True M.I.S. is a medical device that received FDA 510(k) clearance on 2022-09-16. The listed applicant is Innovative Surgical Designs, Inc.. The 510(k) number is K220297.
When did True Tulip, True M.I.S. receive FDA 510(k) clearance?
True Tulip, True M.I.S. received FDA 510(k) clearance on 2022-09-16, under 510(k) number K220297.
Who is the listed applicant for True Tulip, True M.I.S.?
The FDA 510(k) record lists Innovative Surgical Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for True Tulip, True M.I.S.?
The FDA product code for True Tulip, True M.I.S. is NKB.
Other records listing Innovative Surgical Designs, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NKB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.