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FDA 510(k)

STRYKER EXTERNAL FIXATION SYSTEM

K-Number: K071628 · 2007-08-10

ApplicantStryker Cmf
Decision Date2007-08-10
Product CodeMQN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STRYKER EXTERNAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Cmf. It received FDA 510(k) clearance on 2007-08-10 under 510(k) number K071628. The device is classified under product code MQN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER EXTERNAL FIXATION SYSTEM?

STRYKER EXTERNAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2007-08-10. The listed applicant is Stryker Cmf. The 510(k) number is K071628.

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

STRYKER EXTERNAL FIXATION SYSTEM received FDA 510(k) clearance on 2007-08-10, under 510(k) number K071628.

Who is the listed applicant for STRYKER EXTERNAL FIXATION SYSTEM?

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

What is the FDA product code for STRYKER EXTERNAL FIXATION SYSTEM?

The FDA product code for STRYKER EXTERNAL FIXATION SYSTEM is MQN.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stryker Cmf 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.

K060750STRYKER INJECTABLE CEMENT

Related Devices (Code: MQN)

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.

K220050KLS Martin IPS DistractionKLS Martin L.P.K183113DePuy Synthes Maxillofacial Portfolio - MR ConditionalSynthes (USA) Products, LLCK181504Stryker Pediatric Mandibular Distractor 2StrykerK162594Craniomaxillofacial Distraction System (CMFD)Synthes USA Products, LLCK161470Internal Distraction - SterileKLS Martin L.P.K121502SYNTHES CURVILINEAR DISTRACTION SYSTEMSynthes, 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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