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FDA 510(k)

ACROMED BONE PLATE BENDER

K-Number: K872949 · 1987-10-15

ApplicantBuckman Co., Inc.
Decision Date1987-10-15
Product CodeHXW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED BONE PLATE BENDER 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 1987-10-15 under 510(k) number K872949. The device is classified under product code HXW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED BONE PLATE BENDER?

ACROMED BONE PLATE BENDER is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Buckman Co., Inc.. The 510(k) number is K872949.

When did ACROMED BONE PLATE BENDER receive FDA 510(k) clearance?

ACROMED BONE PLATE BENDER received FDA 510(k) clearance on 1987-10-15, under 510(k) number K872949.

Who is the listed applicant for ACROMED BONE PLATE BENDER?

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 PLATE BENDER?

The FDA product code for ACROMED BONE PLATE BENDER is HXW.

Related Clinical Trials

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Other records listing Buckman Co., Inc. as applicant

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.

K961320CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEMK974641FUTURELASE 3000/3002 ERBIUM LASER SYSTEMK964252ORTHOCHUCKK950099SYNERGY(TM) TI POSTERIOR SPINAL SYSTEMK960451WEBB-MORLEY SPINE SYSTEMK950999KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS

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Related Devices (Code: HXW)

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.

K870668DRIVER-BENDER-EXTRACTOR, BONE PINMilitary Engineering, Inc.K870084RD 140 SURGICAL BENDERTerray Manufacturing, 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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