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FDA 510(k)

KNEE AID

K-Number: K760002 · 1976-07-26

ApplicantZimmer, Inc.
Decision Date1976-07-26
Product CodeIQI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KNEE AID is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1976-07-26 under 510(k) number K760002. The device is classified under product code IQI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNEE AID?

KNEE AID is a medical device that received FDA 510(k) clearance on 1976-07-26. The listed applicant is Zimmer, Inc.. The 510(k) number is K760002.

When did KNEE AID receive FDA 510(k) clearance?

KNEE AID received FDA 510(k) clearance on 1976-07-26, under 510(k) number K760002.

Who is the listed applicant for KNEE AID?

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

What is the FDA product code for KNEE AID?

The FDA product code for KNEE AID is IQI.

Other records listing Zimmer, Inc. as applicant

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Related Devices (Code: IQI)

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.

K052771SENSOR WALKOtto Bock Healthcare LPK031576SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1Surgitech, Inc.K926391ACCUFLEX DYNAMIC ELBOW ORTHOSISRegulatory & Marketing Services, Inc.K910974MCCONNELL SHOULDER BRACEMcconnell OrthopedicK874502GAIT-AID ORTHOPEDIC INSOLEGait-Aid, Inc.K831542ADJUSTABLE POLYCENTRIC ELBOW HINGEFred Sammons, Inc.

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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