GERTIE MARX EPI-SPINAL TRAY
K-Number: K943319 · 1995-06-30
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Device Summary
Frequently Asked Questions
What is the GERTIE MARX EPI-SPINAL TRAY?
GERTIE MARX EPI-SPINAL TRAY is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Spinal Specialties, Inc.. The 510(k) number is K943319.
When did GERTIE MARX EPI-SPINAL TRAY receive FDA 510(k) clearance?
GERTIE MARX EPI-SPINAL TRAY received FDA 510(k) clearance on 1995-06-30, under 510(k) number K943319.
Who is the listed applicant for GERTIE MARX EPI-SPINAL TRAY?
The FDA 510(k) record lists Spinal Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GERTIE MARX EPI-SPINAL TRAY?
The FDA product code for GERTIE MARX EPI-SPINAL TRAY is CAZ.
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 Spinal Specialties, 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: CAZ)
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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