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FDA 510(k)

VISTA -S DEVICE

K-Number: K070382 · 2007-05-30

ApplicantZimmer Trabecular Metal Technology
Decision Date2007-05-30
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VISTA -S DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Trabecular Metal Technology. It received FDA 510(k) clearance on 2007-05-30 under 510(k) number K070382. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA -S DEVICE?

VISTA -S DEVICE is a medical device that received FDA 510(k) clearance on 2007-05-30. The listed applicant is Zimmer Trabecular Metal Technology. The 510(k) number is K070382.

When did VISTA -S DEVICE receive FDA 510(k) clearance?

VISTA -S DEVICE received FDA 510(k) clearance on 2007-05-30, under 510(k) number K070382.

Who is the listed applicant for VISTA -S DEVICE?

The FDA 510(k) record lists Zimmer Trabecular Metal Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISTA -S DEVICE?

The FDA product code for VISTA -S DEVICE is MQP.

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Other records listing Zimmer Trabecular Metal Technology 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.

K123602TM ARDIS INTERBODY SYSTEM INSERTERK120990NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIAL CONES PROVISIONALS TO NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIALK113561TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATIONK111983VISTA-S DEVICE MODEL 08/06-401-XXXXX, 08/06-402-XXXXXXK103033TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXXK102896TRABECULAR METAL TIBIAL CONE AUGMENTS

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Related Devices (Code: MQP)

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.

K261810Vertiwedge® Intraosseous SystemFoundation Surgical GroupK261031POSEIDON STSignus Medinzintechnik GmbHK253158VyBrate™ VBR SystemVy Spine, LLCK241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc.K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AGK233359DOMINION Expandable Corpectomy SystemAstura Medical

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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