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FDA 510(k)

MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM

K-Number: K052799 · 2005-12-16

ApplicantBonutti Research, Inc.
Decision Date2005-12-16
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bonutti Research, Inc.. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K052799. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM?

MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Bonutti Research, Inc.. The 510(k) number is K052799.

When did MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM receive FDA 510(k) clearance?

MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM received FDA 510(k) clearance on 2005-12-16, under 510(k) number K052799.

Who is the listed applicant for MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM?

The FDA 510(k) record lists Bonutti Research, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM?

The FDA product code for MULTITAK 6.0 MM ABSORBABLE ANCHOR SYSTEM is MAI.

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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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