SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS
K-Number: K032559 · 2003-10-22
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Device Summary
Frequently Asked Questions
What is the SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS?
SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS is a medical device that received FDA 510(k) clearance on 2003-10-22. The listed applicant is Synthes (Usa). The 510(k) number is K032559.
When did SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS receive FDA 510(k) clearance?
SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS received FDA 510(k) clearance on 2003-10-22, under 510(k) number K032559.
Who is the listed applicant for SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS?
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 4.0MM TITANIUM (TI.) LOCKING SCREWS?
The FDA product code for SYNTHES 4.0MM TITANIUM (TI.) LOCKING SCREWS 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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