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FDA 510(k)

ARCTEC SEMIRIGID PLATING SYSTEM

K-Number: K051044 · 2005-10-07

ApplicantAltiva Corp.
Decision Date2005-10-07
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARCTEC SEMIRIGID PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Altiva Corp.. It received FDA 510(k) clearance on 2005-10-07 under 510(k) number K051044. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARCTEC SEMIRIGID PLATING SYSTEM?

ARCTEC SEMIRIGID PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Altiva Corp.. The 510(k) number is K051044.

When did ARCTEC SEMIRIGID PLATING SYSTEM receive FDA 510(k) clearance?

ARCTEC SEMIRIGID PLATING SYSTEM received FDA 510(k) clearance on 2005-10-07, under 510(k) number K051044.

Who is the listed applicant for ARCTEC SEMIRIGID PLATING SYSTEM?

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

What is the FDA product code for ARCTEC SEMIRIGID PLATING SYSTEM?

The FDA product code for ARCTEC SEMIRIGID PLATING SYSTEM is MNH. This falls under the ENT category.

Related Clinical Trials

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Other records listing Altiva Corp. 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.

K070891ALTIVA CLASSIC ACP SYSTEMK061482ALTES BUTTRESS PLATING SYSTEMK053070CONTOUR II SPINAL SYSTEMK051216HYDRALOK SYSTEM

Related Devices (Code: MNH)

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.

K162066Reliance Spinal Screw SystemReliance Medical Systems, LLCK162801CastleLoc Spinal Fixation SystemL&K BIOMED Co., Ltd.K162143FixxSure® X-LinkInnovasis, Inc.K161151Spinal fixation systemCanwell Medical Co., Ltd.K162189ANAX™ 5.5 Spinal SystemU&I CorporationK151362HC Spinal SystemHung Chun Bio-S Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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