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FDA 510(k)

SYNTHES (USA) CHRONOS-BETA-TCP

K-Number: K053022 · 2006-01-23

ApplicantSynthes (Usa)
Decision Date2006-01-23
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYNTHES (USA) CHRONOS-BETA-TCP is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2006-01-23 under 510(k) number K053022. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES (USA) CHRONOS-BETA-TCP?

SYNTHES (USA) CHRONOS-BETA-TCP is a medical device that received FDA 510(k) clearance on 2006-01-23. The listed applicant is Synthes (Usa). The 510(k) number is K053022.

When did SYNTHES (USA) CHRONOS-BETA-TCP receive FDA 510(k) clearance?

SYNTHES (USA) CHRONOS-BETA-TCP received FDA 510(k) clearance on 2006-01-23, under 510(k) number K053022.

Who is the listed applicant for SYNTHES (USA) CHRONOS-BETA-TCP?

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 (USA) CHRONOS-BETA-TCP?

The FDA product code for SYNTHES (USA) CHRONOS-BETA-TCP is LYC.

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Related Devices (Code: LYC)

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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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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