510(k) K221059

Device
Identity Imprint Knee Replacement System (including Identity Imprint Posterior Stabilized (PS) KRS and Identity Imprint Cruciate Retaining (CR) KRS)
Applicant
Conformis, Inc.
510(k) number
K221059
Product code
JWH
Decision
Substantially Equivalent (SESE)
Decision date
2022-05-10
Date received
2022-04-11
Regulation
888.3560
Classification name
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Kara Johnson
Address
600 Technology Park Dr., 4th Floor Billerica MA US 01821 01821

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code JWH#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K260063GSPE SpacerThe General Hospital Corporation, d/b/a Massachusetts2026-09-11
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K261734Klassic Infection Spacer SystemTotal Joint Orthopedics, Inc.2026-07-23
K261458ATTUNE Total Knee System; ATTUNE Cementless Knee SystemDePuy Ireland UC2026-06-25
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K253314Freedom Infinia™ Total Knee SystemMaxx Orthopedics, Inc.2025-10-29
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