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FDA 510(k)

FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT

K-Number: K911972 · 1991-10-25

ApplicantIntermedics Orthopedics
Decision Date1991-10-25
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1991-10-25 under 510(k) number K911972. 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 FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT?

FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT is a medical device that received FDA 510(k) clearance on 1991-10-25. The listed applicant is Intermedics Orthopedics. The 510(k) number is K911972.

When did FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT receive FDA 510(k) clearance?

FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT received FDA 510(k) clearance on 1991-10-25, under 510(k) number K911972.

Who is the listed applicant for FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT?

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 FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT?

The FDA product code for FREEMAN-SAMUELSON MODULAR TOTAL KNEE REPLACEMENT is JWH.

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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.

K262057GMK ExtensionMedacta International SAK260063GSPE SpacerThe General Hospital Corporation, d/b/a MassachusettsK262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) Co., Ltd.

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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