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FDA 510(k)

METACARPAL FIXATION SYSTEM

K-Number: K991064 · 1999-06-23

ApplicantMedcanica, Inc.
Decision Date1999-06-23
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

METACARPAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medcanica, Inc.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K991064. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METACARPAL FIXATION SYSTEM?

METACARPAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Medcanica, Inc.. The 510(k) number is K991064.

When did METACARPAL FIXATION SYSTEM receive FDA 510(k) clearance?

METACARPAL FIXATION SYSTEM received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991064.

Who is the listed applicant for METACARPAL FIXATION SYSTEM?

The FDA 510(k) record lists Medcanica, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METACARPAL FIXATION SYSTEM?

The FDA product code for METACARPAL FIXATION SYSTEM is HTY.

Related Clinical Trials

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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Other records listing Medcanica, 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.

K011373INSTRUMENT DAMPING PORTK011349INTERCOSTAL LOCKABLE-DIRECTABLE PORTK994232PHALANGEAL FIXATION SYSTEMK991486ULTRA-CBX

Related Devices (Code: HTY)

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.

K262722Primal K-Wire (P99-193-1410)Paragon 28, Inc.K253325ZipToe™ Hammertoe Fusion SystemToetal SolutionsK252657Impact PEEK Union Nail SystemNvision Biomedical Technologies, Inc.K250315RONAVIS – FX (FX-001)AIRS, Inc.K251362PediFlex™ Flexible Nail SystemOrthoPediatrics Corp.K250646Impact PEEK Union Nail SystemNvision Biomedical Technologies

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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