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FDA 510(k)

ACROMED BONE SCREW TAP SLEEVES

K-Number: K873067 · 1987-09-02

ApplicantBuckman Co., Inc.
Decision Date1987-09-02
Product CodeHWX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED BONE SCREW TAP SLEEVES 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 1987-09-02 under 510(k) number K873067. The device is classified under product code HWX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED BONE SCREW TAP SLEEVES?

ACROMED BONE SCREW TAP SLEEVES is a medical device that received FDA 510(k) clearance on 1987-09-02. The listed applicant is Buckman Co., Inc.. The 510(k) number is K873067.

When did ACROMED BONE SCREW TAP SLEEVES receive FDA 510(k) clearance?

ACROMED BONE SCREW TAP SLEEVES received FDA 510(k) clearance on 1987-09-02, under 510(k) number K873067.

Who is the listed applicant for ACROMED BONE SCREW TAP SLEEVES?

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 BONE SCREW TAP SLEEVES?

The FDA product code for ACROMED BONE SCREW TAP SLEEVES is HWX.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: HWX)

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.

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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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