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FDA 510(k)

BIOMET VISION FOOTRING SYSTEM

K-Number: K093057 · 2009-12-01

ApplicantEbi, L.P.
Decision Date2009-12-01
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOMET VISION FOOTRING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ebi, L.P.. It received FDA 510(k) clearance on 2009-12-01 under 510(k) number K093057. 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 BIOMET VISION FOOTRING SYSTEM?

BIOMET VISION FOOTRING SYSTEM is a medical device that received FDA 510(k) clearance on 2009-12-01. The listed applicant is Ebi, L.P.. The 510(k) number is K093057.

When did BIOMET VISION FOOTRING SYSTEM receive FDA 510(k) clearance?

BIOMET VISION FOOTRING SYSTEM received FDA 510(k) clearance on 2009-12-01, under 510(k) number K093057.

Who is the listed applicant for BIOMET VISION FOOTRING SYSTEM?

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

What is the FDA product code for BIOMET VISION FOOTRING SYSTEM?

The FDA product code for BIOMET VISION FOOTRING SYSTEM is KTT.

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Other records listing Ebi, L.P. 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.

K100438POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEMK100220POLARIS SPINAL SYSTEMK093880PEANUT GROWTH CONTROL PLATING SYSTEMK092574ESL SPINAL SYSTEMK092336C-THRU SPINAL SYSTEMK091381IBEX SPINAL SYSTEM

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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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