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FDA 510(k)

DURACON POSTERIOR FEMORAL SPACER

K-Number: K963242 · 1996-11-14

ApplicantHowmedica Corp.
Decision Date1996-11-14
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DURACON POSTERIOR FEMORAL SPACER is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1996-11-14 under 510(k) number K963242. 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 DURACON POSTERIOR FEMORAL SPACER?

DURACON POSTERIOR FEMORAL SPACER is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Howmedica Corp.. The 510(k) number is K963242.

When did DURACON POSTERIOR FEMORAL SPACER receive FDA 510(k) clearance?

DURACON POSTERIOR FEMORAL SPACER received FDA 510(k) clearance on 1996-11-14, under 510(k) number K963242.

Who is the listed applicant for DURACON POSTERIOR FEMORAL SPACER?

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

What is the FDA product code for DURACON POSTERIOR FEMORAL SPACER?

The FDA product code for DURACON POSTERIOR FEMORAL SPACER is JWH.

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Other records listing Howmedica 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.

K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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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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