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FDA 510(k)

QUADRAPLEGIC WALKING AID

K-Number: K772267 · 1977-12-20

Decision Date1977-12-20
Product CodeIPS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUADRAPLEGIC WALKING AID is the device name listed in this FDA 510(k) record. The listed applicant is Med Fusion Systems, Inc.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772267. The device is classified under product code IPS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUADRAPLEGIC WALKING AID?

QUADRAPLEGIC WALKING AID is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Med Fusion Systems, Inc.. The 510(k) number is K772267.

When did QUADRAPLEGIC WALKING AID receive FDA 510(k) clearance?

QUADRAPLEGIC WALKING AID received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772267.

Who is the listed applicant for QUADRAPLEGIC WALKING AID?

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

What is the FDA product code for QUADRAPLEGIC WALKING AID?

The FDA product code for QUADRAPLEGIC WALKING AID is IPS.

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 Med Fusion Systems, 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 22 devices →

Related Devices (Code: IPS)

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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