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FDA 510(k)

FUSE PLIF CAFE

K-Number: K100945 · 2011-02-09

ApplicantAdvanced Medical Technologies AG
Decision Date2011-02-09
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FUSE PLIF CAFE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Technologies AG. It received FDA 510(k) clearance on 2011-02-09 under 510(k) number K100945. 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 FUSE PLIF CAFE?

FUSE PLIF CAFE is a medical device that received FDA 510(k) clearance on 2011-02-09. The listed applicant is Advanced Medical Technologies AG. The 510(k) number is K100945.

When did FUSE PLIF CAFE receive FDA 510(k) clearance?

FUSE PLIF CAFE received FDA 510(k) clearance on 2011-02-09, under 510(k) number K100945.

Who is the listed applicant for FUSE PLIF CAFE?

The FDA 510(k) record lists Advanced Medical Technologies AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FUSE PLIF CAFE?

The FDA product code for FUSE PLIF CAFE is MAX.

Other records listing Advanced Medical Technologies AG as applicant

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Related Devices (Code: MAX)

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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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