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FDA 510(k)

INNESIS PEEK CAGE

K-Number: K120464 · 2013-01-18

ApplicantBk Meditech, Co., Ltd.
Decision Date2013-01-18
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INNESIS PEEK CAGE is the device name listed in this FDA 510(k) record. The listed applicant is Bk Meditech, Co., Ltd.. It received FDA 510(k) clearance on 2013-01-18 under 510(k) number K120464. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNESIS PEEK CAGE?

INNESIS PEEK CAGE is a medical device that received FDA 510(k) clearance on 2013-01-18. The listed applicant is Bk Meditech, Co., Ltd.. The 510(k) number is K120464.

When did INNESIS PEEK CAGE receive FDA 510(k) clearance?

INNESIS PEEK CAGE received FDA 510(k) clearance on 2013-01-18, under 510(k) number K120464.

Who is the listed applicant for INNESIS PEEK CAGE?

The FDA 510(k) record lists Bk Meditech, Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INNESIS PEEK CAGE?

The FDA product code for INNESIS PEEK CAGE is MAX.

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Related Devices (Code: MAX)

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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