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FDA 510(k)

THE NATURAL-KNEE REVISION

K-Number: K930554 · 1993-09-21

ApplicantIntermedics Orthopedics
Decision Date1993-09-21
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE NATURAL-KNEE REVISION is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1993-09-21 under 510(k) number K930554. 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 THE NATURAL-KNEE REVISION?

THE NATURAL-KNEE REVISION is a medical device that received FDA 510(k) clearance on 1993-09-21. The listed applicant is Intermedics Orthopedics. The 510(k) number is K930554.

When did THE NATURAL-KNEE REVISION receive FDA 510(k) clearance?

THE NATURAL-KNEE REVISION received FDA 510(k) clearance on 1993-09-21, under 510(k) number K930554.

Who is the listed applicant for THE NATURAL-KNEE REVISION?

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

What is the FDA product code for THE NATURAL-KNEE REVISION?

The FDA product code for THE NATURAL-KNEE REVISION 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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