Identity Imprint Cruciate Retaining (CR) Knee Replacement System and Identity Imprint Posterior Stabilized (PS) Knee Rep
Summary
Conformis, Inc. received 510(k) clearance for Identity Imprint Cruciate Retaining (CR) Knee Replacement System and Identity Imprint Posterior Stabilized (PS) Knee Replacement System, a JWH device. Cleared on 2021-11-10.
Details
Source
510(k) Clearance
External ID
K213389
Action Date
2021-11-10
Status
Special
Category
device
Product Code
JWH
Product Description
Identity Imprint Cruciate Retaining (CR) Knee Replacement System and Identity Imprint Posterior Stabilized (PS) Knee Replacement System. Product code: JWH.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Conformis, Inc. has received 11 total clearances in our database.
Conformis, Inc. has 16 FDA actions in our database, including 5 recalls and 11 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Conformis, Inc. have FDA actions?
Conformis, Inc. has 16 FDA actions in our database, including 5 recalls and 11 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K213389" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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