SPI SYSTEM DENTAL IMPLANTS
K-Number: K072649 · 2007-12-06
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Device Summary
Frequently Asked Questions
What is the SPI SYSTEM DENTAL IMPLANTS?
SPI SYSTEM DENTAL IMPLANTS is a medical device that received FDA 510(k) clearance on 2007-12-06. The listed applicant is Thommen Medical AG. The 510(k) number is K072649.
When did SPI SYSTEM DENTAL IMPLANTS receive FDA 510(k) clearance?
SPI SYSTEM DENTAL IMPLANTS received FDA 510(k) clearance on 2007-12-06, under 510(k) number K072649.
Who is the listed applicant for SPI SYSTEM DENTAL IMPLANTS?
The FDA 510(k) record lists Thommen Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPI SYSTEM DENTAL IMPLANTS?
The FDA product code for SPI SYSTEM DENTAL IMPLANTS is DZE.
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 Thommen Medical AG 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: DZE)
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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