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FDA 510(k)

BIRDIE BRACKET

K-Number: K872028 · 1987-07-31

ApplicantWilliam W. Wilkerson & Gregory A. Knutson
Decision Date1987-07-31
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BIRDIE BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is William W. Wilkerson & Gregory A. Knutson. It received FDA 510(k) clearance on 1987-07-31 under 510(k) number K872028. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIRDIE BRACKET?

BIRDIE BRACKET is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is William W. Wilkerson & Gregory A. Knutson. The 510(k) number is K872028.

When did BIRDIE BRACKET receive FDA 510(k) clearance?

BIRDIE BRACKET received FDA 510(k) clearance on 1987-07-31, under 510(k) number K872028.

Who is the listed applicant for BIRDIE BRACKET?

The FDA 510(k) record lists William W. Wilkerson & Gregory A. Knutson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIRDIE BRACKET?

The FDA product code for BIRDIE BRACKET is ISA.

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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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