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FDA 510(k)

HASTING FINGER FIXATOR INSTRUMENTS

K-Number: K880046 · 1988-02-16

ApplicantBuckman Co., Inc.
Decision Date1988-02-16
Product CodeHXY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HASTING FINGER FIXATOR INSTRUMENTS 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 1988-02-16 under 510(k) number K880046. The device is classified under product code HXY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HASTING FINGER FIXATOR INSTRUMENTS?

HASTING FINGER FIXATOR INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is Buckman Co., Inc.. The 510(k) number is K880046.

When did HASTING FINGER FIXATOR INSTRUMENTS receive FDA 510(k) clearance?

HASTING FINGER FIXATOR INSTRUMENTS received FDA 510(k) clearance on 1988-02-16, under 510(k) number K880046.

Who is the listed applicant for HASTING FINGER FIXATOR INSTRUMENTS?

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 HASTING FINGER FIXATOR INSTRUMENTS?

The FDA product code for HASTING FINGER FIXATOR INSTRUMENTS is HXY.

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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: HXY)

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.

K923776BENDEREV DRILL GUIDENeimark Labs, Inc.K892904MITEK DRILL GUIDEMitek Surgical Products, Inc.K880264BONE SUTURE FIXATION DEVICEOrthopedic Systems, Inc.K880381TELOS DISTAL TARGETING DEVICEAustin Assoc.K831043ANDREWS REMOTE CHUCK DRILLOrthopedic Systems, Inc.K770204CEMENT EXTRACTOR DRILLDepuy, 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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