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FDA 510(k)

SPECIALIST(R) WALKER

K-Number: K924984 · 1993-02-01

ApplicantJohnson & Johnson Orthopaedics, Inc.
Decision Date1993-02-01
Product CodeFYH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPECIALIST(R) WALKER is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Orthopaedics, Inc.. It received FDA 510(k) clearance on 1993-02-01 under 510(k) number K924984. The device is classified under product code FYH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIALIST(R) WALKER?

SPECIALIST(R) WALKER is a medical device that received FDA 510(k) clearance on 1993-02-01. The listed applicant is Johnson & Johnson Orthopaedics, Inc.. The 510(k) number is K924984.

When did SPECIALIST(R) WALKER receive FDA 510(k) clearance?

SPECIALIST(R) WALKER received FDA 510(k) clearance on 1993-02-01, under 510(k) number K924984.

Who is the listed applicant for SPECIALIST(R) WALKER?

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

What is the FDA product code for SPECIALIST(R) WALKER?

The FDA product code for SPECIALIST(R) WALKER is FYH.

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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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