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FDA 510(k)

ACROMED ADS BONE NAIL DRIVER

K-Number: K875054 · 1988-01-28

ApplicantBuckman Co., Inc.
Decision Date1988-01-28
Product CodeHWR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED ADS BONE NAIL DRIVER 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 1988-01-28 under 510(k) number K875054. The device is classified under product code HWR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED ADS BONE NAIL DRIVER?

ACROMED ADS BONE NAIL DRIVER is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Buckman Co., Inc.. The 510(k) number is K875054.

When did ACROMED ADS BONE NAIL DRIVER receive FDA 510(k) clearance?

ACROMED ADS BONE NAIL DRIVER received FDA 510(k) clearance on 1988-01-28, under 510(k) number K875054.

Who is the listed applicant for ACROMED ADS BONE NAIL DRIVER?

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 ADS BONE NAIL DRIVER?

The FDA product code for ACROMED ADS BONE NAIL DRIVER is HWR.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: HWR)

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K915776KNEE PROSTHESIS DRIVERKim-Med, Inc.K870848SCHULTZ METACARPAL COMPONENT DRIVERWarsaw Orthopedic, Inc.K870847SCHULTZ PHALANGEAL COMPONENT DRIVERWarsaw Orthopedic, Inc.

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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