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FDA 510(k)

MULTITAK SS

K-Number: K993115 · 1999-12-17

ApplicantBonutti Research, Inc.
Decision Date1999-12-17
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULTITAK SS 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 1999-12-17 under 510(k) number K993115. 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 SS?

MULTITAK SS is a medical device that received FDA 510(k) clearance on 1999-12-17. The listed applicant is Bonutti Research, Inc.. The 510(k) number is K993115.

When did MULTITAK SS receive FDA 510(k) clearance?

MULTITAK SS received FDA 510(k) clearance on 1999-12-17, under 510(k) number K993115.

Who is the listed applicant for MULTITAK SS?

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 SS?

The FDA product code for MULTITAK SS 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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