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FDA 510(k)

Precision Casting Solutions Total Knee System

K-Number: K190355 · 2019-05-16

ApplicantPrecision Casting Solutions, Inc.
Decision Date2019-05-16
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Precision Casting Solutions Total Knee System is the device name listed in this FDA 510(k) record. The listed applicant is Precision Casting Solutions, Inc.. It received FDA 510(k) clearance on 2019-05-16 under 510(k) number K190355. 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 Precision Casting Solutions Total Knee System?

Precision Casting Solutions Total Knee System is a medical device that received FDA 510(k) clearance on 2019-05-16. The listed applicant is Precision Casting Solutions, Inc.. The 510(k) number is K190355.

When did Precision Casting Solutions Total Knee System receive FDA 510(k) clearance?

Precision Casting Solutions Total Knee System received FDA 510(k) clearance on 2019-05-16, under 510(k) number K190355.

Who is the listed applicant for Precision Casting Solutions Total Knee System?

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

What is the FDA product code for Precision Casting Solutions Total Knee System?

The FDA product code for Precision Casting Solutions Total Knee System is JWH.

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.

K261563Freedom Total Knee System (E-Poly Tibial Liners)Maxx Orthopedics, Inc.K262251ACTIFY™ Total Knee System, ACTIFY™ 3D Total Knee System (ACTIFY MC Tibial Insert)Globus Medical, Inc.K261734Klassic Infection Spacer SystemTotal Joint Orthopedics, Inc.K261458ATTUNE Total Knee System; ATTUNE Cementless Knee SystemDePuy Ireland UCK261032NovoKnee (SteriKnee)NovoSourceK253793Materialise TKA Guide SystemMaterialise NV

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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