Worrell Patella Femoral Shield
FDA 510(k) K801934 · Depuy, Inc.
510(k) numberK801934
Submission
- Device name
- Worrell Patella Femoral Shield
- Applicant
- Depuy, Inc.
Mchenry, IL, US - Received
- August 12, 1980
- Decision date
- November 13, 1980
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Worrell Patella Femoral Shield cleared by the FDA?
Worrell Patella Femoral Shield (K801934) received a 510(k) decision of Substantially Equivalent on November 13, 1980, 93 days after the submission was received.