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FDA 510(k)

KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED

K-Number: K874547 · 1987-12-18

Decision Date1987-12-18
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1987-12-18 under 510(k) number K874547. 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 KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED?

KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED is a medical device that received FDA 510(k) clearance on 1987-12-18. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K874547.

When did KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED receive FDA 510(k) clearance?

KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED received FDA 510(k) clearance on 1987-12-18, under 510(k) number K874547.

Who is the listed applicant for KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED?

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

What is the FDA product code for KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED?

The FDA product code for KIRSCHNER PERFORM TOTAL KNEE SYSTEM POROUS COATED is JWH.

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 Kirschner Medical Corp. 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 76 devices →

Related Devices (Code: JWH)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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