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FDA 510(k)

ACE/WILLIAMS MICROSURGERY SAW SYSTEM

K-Number: K902525 · 1990-11-26

ApplicantBuckman Co., Inc.
Decision Date1990-11-26
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACE/WILLIAMS MICROSURGERY SAW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1990-11-26 under 510(k) number K902525. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE/WILLIAMS MICROSURGERY SAW SYSTEM?

ACE/WILLIAMS MICROSURGERY SAW SYSTEM is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Buckman Co., Inc.. The 510(k) number is K902525.

When did ACE/WILLIAMS MICROSURGERY SAW SYSTEM receive FDA 510(k) clearance?

ACE/WILLIAMS MICROSURGERY SAW SYSTEM received FDA 510(k) clearance on 1990-11-26, under 510(k) number K902525.

Who is the listed applicant for ACE/WILLIAMS MICROSURGERY SAW SYSTEM?

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

What is the FDA product code for ACE/WILLIAMS MICROSURGERY SAW SYSTEM?

The FDA product code for ACE/WILLIAMS MICROSURGERY SAW SYSTEM is HWE.

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Related Devices (Code: HWE)

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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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