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FDA 510(k)

VANDERBILT BLADE HOLDER

K-Number: K761097 · 1976-11-30

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-11-30
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VANDERBILT BLADE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1976-11-30 under 510(k) number K761097. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANDERBILT BLADE HOLDER?

VANDERBILT BLADE HOLDER is a medical device that received FDA 510(k) clearance on 1976-11-30. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K761097.

When did VANDERBILT BLADE HOLDER receive FDA 510(k) clearance?

VANDERBILT BLADE HOLDER received FDA 510(k) clearance on 1976-11-30, under 510(k) number K761097.

Who is the listed applicant for VANDERBILT BLADE HOLDER?

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

What is the FDA product code for VANDERBILT BLADE HOLDER?

The FDA product code for VANDERBILT BLADE HOLDER is HAO.

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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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