SYNTHES PROXIMAL HUMERAL NAIL
K-Number: K002729 · 2000-10-06
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Device Summary
Frequently Asked Questions
What is the SYNTHES PROXIMAL HUMERAL NAIL?
SYNTHES PROXIMAL HUMERAL NAIL is a medical device that received FDA 510(k) clearance on 2000-10-06. The listed applicant is Synthes (Usa). The 510(k) number is K002729.
When did SYNTHES PROXIMAL HUMERAL NAIL receive FDA 510(k) clearance?
SYNTHES PROXIMAL HUMERAL NAIL received FDA 510(k) clearance on 2000-10-06, under 510(k) number K002729.
Who is the listed applicant for SYNTHES PROXIMAL HUMERAL NAIL?
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 PROXIMAL HUMERAL NAIL?
The FDA product code for SYNTHES PROXIMAL HUMERAL NAIL is JDS.
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: JDS)
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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