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FDA 510(k)

WEBB-MORLEY SPINE SYSTEM

K-Number: K960451 · 1996-04-18

Decision Date1996-04-18
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

WEBB-MORLEY SPINE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1996-04-18 under 510(k) number K960451. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WEBB-MORLEY SPINE SYSTEM?

WEBB-MORLEY SPINE SYSTEM is a medical device that received FDA 510(k) clearance on 1996-04-18. The listed applicant is Buckman Co., Inc.. The 510(k) number is K960451.

When did WEBB-MORLEY SPINE SYSTEM receive FDA 510(k) clearance?

WEBB-MORLEY SPINE SYSTEM received FDA 510(k) clearance on 1996-04-18, under 510(k) number K960451.

Who is the listed applicant for WEBB-MORLEY SPINE SYSTEM?

The FDA 510(k) record lists Buckman Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEBB-MORLEY SPINE SYSTEM?

The FDA product code for WEBB-MORLEY SPINE SYSTEM is MNH. This falls under the ENT category.

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 Buckman Co., 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 111 devices →

Related Devices (Code: MNH)

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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