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FDA 510(k)

TAYLOR SPINAL RETRACTOR

K-Number: K892546 · 1989-05-11

Decision Date1989-05-11
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TAYLOR SPINAL RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-05-11 under 510(k) number K892546. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 76 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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