TAYLOR SPINAL RETRACTOR
K-Number: K892546 · 1989-05-11
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Device Summary
Frequently Asked Questions
What is the TAYLOR SPINAL RETRACTOR?
TAYLOR SPINAL RETRACTOR is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K892546.
When did TAYLOR SPINAL RETRACTOR receive FDA 510(k) clearance?
TAYLOR SPINAL RETRACTOR received FDA 510(k) clearance on 1989-05-11, under 510(k) number K892546.
Who is the listed applicant for TAYLOR SPINAL RETRACTOR?
The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAYLOR SPINAL RETRACTOR?
The FDA product code for TAYLOR SPINAL RETRACTOR is HAO.
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 Zinnanti Surgical Instruments, 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: HAO)
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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