ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED
K-Number: K024111 · 2003-06-10
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Device Summary
Frequently Asked Questions
What is the ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED?
ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED is a medical device that received FDA 510(k) clearance on 2003-06-10. The listed applicant is Astra Tech, Inc.. The 510(k) number is K024111.
When did ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED receive FDA 510(k) clearance?
ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED received FDA 510(k) clearance on 2003-06-10, under 510(k) number K024111.
Who is the listed applicant for ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED?
The FDA 510(k) record lists Astra Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED?
The FDA product code for ASTRA TECH IMPLANTS-DENTAL SYSTEM FIXTURE OSSEOSPEED 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 Astra Tech, 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: 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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