THORACIC ANTERIOR SPINAL FIXATION PLATE
K-Number: K910874 · 1992-02-03
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Device Summary
Frequently Asked Questions
What is the THORACIC ANTERIOR SPINAL FIXATION PLATE?
THORACIC ANTERIOR SPINAL FIXATION PLATE is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Terray Manufacturing, Inc.. The 510(k) number is K910874.
When did THORACIC ANTERIOR SPINAL FIXATION PLATE receive FDA 510(k) clearance?
THORACIC ANTERIOR SPINAL FIXATION PLATE received FDA 510(k) clearance on 1992-02-03, under 510(k) number K910874.
Who is the listed applicant for THORACIC ANTERIOR SPINAL FIXATION PLATE?
The FDA 510(k) record lists Terray Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THORACIC ANTERIOR SPINAL FIXATION PLATE?
The FDA product code for THORACIC ANTERIOR SPINAL FIXATION PLATE is KWQ.
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.
Other records listing Terray Manufacturing, 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.
Related Devices (Code: KWQ)
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.
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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