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FDA 510(k)

ACROMED WALLIE-HEINIG OSTEOTOMES

K-Number: K870780 · 1987-03-09

ApplicantBuckman Co., Inc.
Decision Date1987-03-09
Product CodeHWM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACROMED WALLIE-HEINIG OSTEOTOMES 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 1987-03-09 under 510(k) number K870780. The device is classified under product code HWM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED WALLIE-HEINIG OSTEOTOMES?

ACROMED WALLIE-HEINIG OSTEOTOMES is a medical device that received FDA 510(k) clearance on 1987-03-09. The listed applicant is Buckman Co., Inc.. The 510(k) number is K870780.

When did ACROMED WALLIE-HEINIG OSTEOTOMES receive FDA 510(k) clearance?

ACROMED WALLIE-HEINIG OSTEOTOMES received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870780.

Who is the listed applicant for ACROMED WALLIE-HEINIG OSTEOTOMES?

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 ACROMED WALLIE-HEINIG OSTEOTOMES?

The FDA product code for ACROMED WALLIE-HEINIG OSTEOTOMES is HWM.

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Related Devices (Code: HWM)

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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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