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FDA 510(k)

SUPERCABLE GRIP AND PLATE SYSTEM

K-Number: K072250 · 2007-11-09

ApplicantKinamed, Inc.
Decision Date2007-11-09
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SUPERCABLE GRIP AND PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 2007-11-09 under 510(k) number K072250. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERCABLE GRIP AND PLATE SYSTEM?

SUPERCABLE GRIP AND PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-09. The listed applicant is Kinamed, Inc.. The 510(k) number is K072250.

When did SUPERCABLE GRIP AND PLATE SYSTEM receive FDA 510(k) clearance?

SUPERCABLE GRIP AND PLATE SYSTEM received FDA 510(k) clearance on 2007-11-09, under 510(k) number K072250.

Who is the listed applicant for SUPERCABLE GRIP AND PLATE SYSTEM?

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

What is the FDA product code for SUPERCABLE GRIP AND PLATE SYSTEM?

The FDA product code for SUPERCABLE GRIP AND PLATE SYSTEM is KTT.

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Other records listing Kinamed, 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.

K122049NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEMK050897NAVIPRO SHOULDER SOFTWARE MODULEK033668NAVIPRO KNEE SOFTWARE MODULEK032950GEM INSET PATELLAR COMPONENTK030256ISO-ELASTIC CERCLAGE SYSTEMK020764NAVIPRO

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Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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