SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE
K-Number: K915818 · 1992-01-17
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Device Summary
Frequently Asked Questions
What is the SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE?
SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE is a medical device that received FDA 510(k) clearance on 1992-01-17. The listed applicant is Synthes (Usa). The 510(k) number is K915818.
When did SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE receive FDA 510(k) clearance?
SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE received FDA 510(k) clearance on 1992-01-17, under 510(k) number K915818.
Who is the listed applicant for SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE?
The FDA 510(k) record lists Synthes (Usa) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE?
The FDA product code for SYNTHES(R) TITANIUM SMALL RECONSTRUCTION PLATE is HRS.
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 Synthes (Usa) 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: HRS)
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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