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FDA 510(k)

SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM

K-Number: K001296 · 2000-07-17

ApplicantCavendish Scott, Inc.
Decision Date2000-07-17
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cavendish Scott, Inc.. It received FDA 510(k) clearance on 2000-07-17 under 510(k) number K001296. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM?

SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is Cavendish Scott, Inc.. The 510(k) number is K001296.

When did SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM receive FDA 510(k) clearance?

SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM received FDA 510(k) clearance on 2000-07-17, under 510(k) number K001296.

Who is the listed applicant for SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM?

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

What is the FDA product code for SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM?

The FDA product code for SPINAL CORD AND IMMOBILIZATION TRACTION SYSTEM is ITH.

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Related Devices (Code: ITH)

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.

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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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