HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE
K-Number: K944905 · 1995-06-07
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Device Summary
Frequently Asked Questions
What is the HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE?
HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 1995-06-07. The listed applicant is Holgrath Medical Technologies, Inc.. The 510(k) number is K944905.
When did HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE receive FDA 510(k) clearance?
HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE received FDA 510(k) clearance on 1995-06-07, under 510(k) number K944905.
Who is the listed applicant for HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE?
The FDA 510(k) record lists Holgrath Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE?
The FDA product code for HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE is BSP.
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 Holgrath Medical Technologies, 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: BSP)
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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