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FDA 510(k)

ACROMED ILIAC SCREW

K-Number: K884161 · 1989-05-03

ApplicantBuckman Co., Inc.
Decision Date1989-05-03
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

ACROMED ILIAC SCREW 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 1989-05-03 under 510(k) number K884161. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ACROMED ILIAC SCREW?

ACROMED ILIAC SCREW is a medical device that received FDA 510(k) clearance on 1989-05-03. The listed applicant is Buckman Co., Inc.. The 510(k) number is K884161.

When did ACROMED ILIAC SCREW receive FDA 510(k) clearance?

ACROMED ILIAC SCREW received FDA 510(k) clearance on 1989-05-03, under 510(k) number K884161.

Who is the listed applicant for ACROMED ILIAC SCREW?

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 ILIAC SCREW?

The FDA product code for ACROMED ILIAC SCREW is KWP.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: KWP)

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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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