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Amedica (AMDA) Receives FDA 510(k) Premarket Notification for Valeo II Interbody Fusion Device System

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Amedica (AMDA) Announces Receipt of FDA Clearance for Expanded Valeo II Lateral Lumbar Sizes

August 24, 2016 9:03 AM EDT

Amedica Corporation (Nasdaq: AMDA) announced the U.S. Food and Drug Administration (FDA) clearance of expanded Valeo II Lateral Lumbar sizes. The additional sizes of the Valeo II LL interbody fusion device will be commercially available August 29, 2016.

The Valeo II LL interbody fusion device is made entirely of Amedica's proprietary medical grade silicon nitride ceramic -- an ideal material for fusion, due to its inherent osteoconductivity, anti-infective properties, bone-like imaging... More

Amedica (AMDA) Active, Shares Gain

August 22, 2016 3:21 PM EDT

Amedica (NASDAQ: AMDA) Active, Shares Gain

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Amedica (AMDA) Receives Nasdaq Listing Notification

August 22, 2016 6:42 AM EDT

Amedica Corporation (Nasdaq: AMDA) announced that on August 17, 2016, the Company received a letter from the Nasdaq Listings Qualifications department of the Nasdaq Capital Market ("Nasdaq") notifying the Company that the minimum bid price per share for its common stock was below $1.00 for a period of thirty (30) consecutive business days and that the Company did not meet the minimum bid price requirement set forth in Nasdaq Listing Rule 5550(a)(2).

The Nasdaq notification... More