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FDA 510(k)

OSTEOMILL BONE GRINDER

K-Number: K861164 · 1986-05-02

ApplicantBiodynamic Technologies, Inc.
Decision Date1986-05-02
Product CodeLYS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEOMILL BONE GRINDER is the device name listed in this FDA 510(k) record. The listed applicant is Biodynamic Technologies, Inc.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K861164. The device is classified under product code LYS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEOMILL BONE GRINDER?

OSTEOMILL BONE GRINDER is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Biodynamic Technologies, Inc.. The 510(k) number is K861164.

When did OSTEOMILL BONE GRINDER receive FDA 510(k) clearance?

OSTEOMILL BONE GRINDER received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861164.

Who is the listed applicant for OSTEOMILL BONE GRINDER?

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

What is the FDA product code for OSTEOMILL BONE GRINDER?

The FDA product code for OSTEOMILL BONE GRINDER is LYS.

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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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