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FDA 510(k)

SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS

K-Number: K040765 · 2004-04-12

ApplicantSynthes (Usa)
Decision Date2004-04-12
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2004-04-12 under 510(k) number K040765. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS?

SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS is a medical device that received FDA 510(k) clearance on 2004-04-12. The listed applicant is Synthes (Usa). The 510(k) number is K040765.

When did SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS receive FDA 510(k) clearance?

SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS received FDA 510(k) clearance on 2004-04-12, under 510(k) number K040765.

Who is the listed applicant for SYNTHES 5.0/7.3 MM CANNULATED 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 5.0/7.3 MM CANNULATED LOCKING SCREWS?

The FDA product code for SYNTHES 5.0/7.3 MM CANNULATED LOCKING SCREWS is JDW.

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.

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Related Devices (Code: JDW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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