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FDA 510(k)

CERADRILL

K-Number: K071352 · 2007-06-29

ApplicantGebr. Brasseler GmbH & Co. KG
Decision Date2007-06-29
Product CodeEJL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERADRILL is the device name listed in this FDA 510(k) record. The listed applicant is Gebr. Brasseler GmbH & Co. KG. It received FDA 510(k) clearance on 2007-06-29 under 510(k) number K071352. The device is classified under product code EJL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERADRILL?

CERADRILL is a medical device that received FDA 510(k) clearance on 2007-06-29. The listed applicant is Gebr. Brasseler GmbH & Co. KG. The 510(k) number is K071352.

When did CERADRILL receive FDA 510(k) clearance?

CERADRILL received FDA 510(k) clearance on 2007-06-29, under 510(k) number K071352.

Who is the listed applicant for CERADRILL?

The FDA 510(k) record lists Gebr. Brasseler GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERADRILL?

The FDA product code for CERADRILL is EJL.

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Other records listing Gebr. Brasseler GmbH & Co. KG 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: EJL)

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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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