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FDA 510(k)

MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS

K-Number: K930831 · 1993-11-16

ApplicantZimmer, Inc.
Decision Date1993-11-16
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1993-11-16 under 510(k) number K930831. 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 MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS?

MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS is a medical device that received FDA 510(k) clearance on 1993-11-16. The listed applicant is Zimmer, Inc.. The 510(k) number is K930831.

When did MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS receive FDA 510(k) clearance?

MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS received FDA 510(k) clearance on 1993-11-16, under 510(k) number K930831.

Who is the listed applicant for MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS?

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

What is the FDA product code for MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS?

The FDA product code for MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS is JWH.

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Other records listing Zimmer, Inc. as applicant

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K262955OsseoFit Stemless Shoulder SystemK260831Z1 Hip SystemK261683Augment Off-Axis Instrument SystemK251840Zimmer® Persona® Personalized Knee SystemK260182Avenir® Müller Stem; Avenir Complete™ Hip SystemK253592Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)

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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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