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FDA 510(k)

CAMCERAM TCP

K-Number: K050357 · 2005-04-21

Decision Date2005-04-21
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAMCERAM TCP is the device name listed in this FDA 510(k) record. The listed applicant is Cam Implants B.V.. It received FDA 510(k) clearance on 2005-04-21 under 510(k) number K050357. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMCERAM TCP?

CAMCERAM TCP is a medical device that received FDA 510(k) clearance on 2005-04-21. The listed applicant is Cam Implants B.V.. The 510(k) number is K050357.

When did CAMCERAM TCP receive FDA 510(k) clearance?

CAMCERAM TCP received FDA 510(k) clearance on 2005-04-21, under 510(k) number K050357.

Who is the listed applicant for CAMCERAM TCP?

The FDA 510(k) record lists Cam Implants B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAMCERAM TCP?

The FDA product code for CAMCERAM TCP is MQV.

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.

Related Devices (Code: MQV)

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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