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FDA 510(k)

LUMBO-SACRAL FLEXION ORTHOSIS

K-Number: K811494 · 1981-06-16

Decision Date1981-06-16
Product CodeIPY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LUMBO-SACRAL FLEXION ORTHOSIS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Appliance Industries, Inc.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811494. The device is classified under product code IPY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMBO-SACRAL FLEXION ORTHOSIS?

LUMBO-SACRAL FLEXION ORTHOSIS is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Surgical Appliance Industries, Inc.. The 510(k) number is K811494.

When did LUMBO-SACRAL FLEXION ORTHOSIS receive FDA 510(k) clearance?

LUMBO-SACRAL FLEXION ORTHOSIS received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811494.

Who is the listed applicant for LUMBO-SACRAL FLEXION ORTHOSIS?

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

What is the FDA product code for LUMBO-SACRAL FLEXION ORTHOSIS?

The FDA product code for LUMBO-SACRAL FLEXION ORTHOSIS is IPY.

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 Surgical Appliance Industries, 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 9 devices →

Related Devices (Code: IPY)

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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