NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS
K-Number: K112616 · 2013-02-08
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Device Summary
Frequently Asked Questions
What is the NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS?
NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS is a medical device that received FDA 510(k) clearance on 2013-02-08. The listed applicant is Heinz Kurz GmbH Medizintechnik. The 510(k) number is K112616.
When did NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS receive FDA 510(k) clearance?
NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS received FDA 510(k) clearance on 2013-02-08, under 510(k) number K112616.
Who is the listed applicant for NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS?
The FDA 510(k) record lists Heinz Kurz GmbH Medizintechnik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS?
The FDA product code for NITIBOND STAPES PROSTHESIS, NITIPLAST STAPES PROSTHESIS is ETB.
Related Clinical Trials
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.
Other records listing Heinz Kurz GmbH Medizintechnik 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: ETB)
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.
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