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FDA 510(k)

POROUS COATED TITANIUM KNEE PROSTHES-

K-Number: K843907 · 1985-01-10

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1985-01-10
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POROUS COATED TITANIUM KNEE PROSTHES- is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1985-01-10 under 510(k) number K843907. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POROUS COATED TITANIUM KNEE PROSTHES-?

POROUS COATED TITANIUM KNEE PROSTHES- is a medical device that received FDA 510(k) clearance on 1985-01-10. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K843907.

When did POROUS COATED TITANIUM KNEE PROSTHES- receive FDA 510(k) clearance?

POROUS COATED TITANIUM KNEE PROSTHES- received FDA 510(k) clearance on 1985-01-10, under 510(k) number K843907.

Who is the listed applicant for POROUS COATED TITANIUM KNEE PROSTHES-?

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

What is the FDA product code for POROUS COATED TITANIUM KNEE PROSTHES-?

The FDA product code for POROUS COATED TITANIUM KNEE PROSTHES- is JWH.

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Related Devices (Code: JWH)

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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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