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FDA 510(k)

RC BUTTRESS

K-Number: K991009 · 1999-06-23

ApplicantBiomet, Inc.
Decision Date1999-06-23
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RC BUTTRESS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K991009. 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 RC BUTTRESS?

RC BUTTRESS is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Biomet, Inc.. The 510(k) number is K991009.

When did RC BUTTRESS receive FDA 510(k) clearance?

RC BUTTRESS received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991009.

Who is the listed applicant for RC BUTTRESS?

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

What is the FDA product code for RC BUTTRESS?

The FDA product code for RC BUTTRESS 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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