RN SYNOCTA TEMPORARY MESO ABUTMENT
K-Number: K051717 · 2005-07-07
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Device Summary
Frequently Asked Questions
What is the RN SYNOCTA TEMPORARY MESO ABUTMENT?
RN SYNOCTA TEMPORARY MESO ABUTMENT is a medical device that received FDA 510(k) clearance on 2005-07-07. The listed applicant is Institut Straumann SA. The 510(k) number is K051717.
When did RN SYNOCTA TEMPORARY MESO ABUTMENT receive FDA 510(k) clearance?
RN SYNOCTA TEMPORARY MESO ABUTMENT received FDA 510(k) clearance on 2005-07-07, under 510(k) number K051717.
Who is the listed applicant for RN SYNOCTA TEMPORARY MESO ABUTMENT?
The FDA 510(k) record lists Institut Straumann SA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RN SYNOCTA TEMPORARY MESO ABUTMENT?
The FDA product code for RN SYNOCTA TEMPORARY MESO ABUTMENT is NHA.
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 Institut Straumann SA 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: NHA)
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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