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FDA 510(k)

AESCULAP BONE MILL

K-Number: K860016 · 1986-03-19

ApplicantAesculap Instruments Corp.
Decision Date1986-03-19
Product CodeLYS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AESCULAP BONE MILL is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Instruments Corp.. It received FDA 510(k) clearance on 1986-03-19 under 510(k) number K860016. 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 AESCULAP BONE MILL?

AESCULAP BONE MILL is a medical device that received FDA 510(k) clearance on 1986-03-19. The listed applicant is Aesculap Instruments Corp.. The 510(k) number is K860016.

When did AESCULAP BONE MILL receive FDA 510(k) clearance?

AESCULAP BONE MILL received FDA 510(k) clearance on 1986-03-19, under 510(k) number K860016.

Who is the listed applicant for AESCULAP BONE MILL?

The FDA 510(k) record lists Aesculap Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AESCULAP BONE MILL?

The FDA product code for AESCULAP BONE MILL is LYS.

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Other records listing Aesculap Instruments Corp. as applicant

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Related Devices (Code: LYS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K883183TRACER BONE MILLDe Medica Mfg., Inc.K860356ORTHOBLEND POWERED BONE MILLZimmer, Inc.K861164OSTEOMILL BONE GRINDERBiodynamic Technologies, Inc.

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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