MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT
K-Number: K941717 · 1995-02-14
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Device Summary
Frequently Asked Questions
What is the MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT?
MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Miguel Martinez M.D.. The 510(k) number is K941717.
When did MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT receive FDA 510(k) clearance?
MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT received FDA 510(k) clearance on 1995-02-14, under 510(k) number K941717.
Who is the listed applicant for MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT?
The FDA 510(k) record lists Miguel Martinez M.D. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT?
The FDA product code for MARTINEZ HYDROXYLAPATITE ORBITAL IMPLANT is HPZ.
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 Miguel Martinez M.D. 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: HPZ)
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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