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FDA 510(k)

ACROMED INTERBODY DEPTH GAUGES

K-Number: K873191 · 1987-09-09

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

Device Summary

ACROMED INTERBODY DEPTH GAUGES 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 1987-09-09 under 510(k) number K873191. The device is classified under product code HTJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED INTERBODY DEPTH GAUGES?

ACROMED INTERBODY DEPTH GAUGES is a medical device that received FDA 510(k) clearance on 1987-09-09. The listed applicant is Buckman Co., Inc.. The 510(k) number is K873191.

When did ACROMED INTERBODY DEPTH GAUGES receive FDA 510(k) clearance?

ACROMED INTERBODY DEPTH GAUGES received FDA 510(k) clearance on 1987-09-09, under 510(k) number K873191.

Who is the listed applicant for ACROMED INTERBODY DEPTH GAUGES?

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 INTERBODY DEPTH GAUGES?

The FDA product code for ACROMED INTERBODY DEPTH GAUGES is HTJ.

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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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