UNIVATION UNICONDYLAR KNEE SYSTEM— 510(k) K081293

Substantially Equivalent

Aesculap Implant Systems, Inc.

FDA 510(k) clearance K081293 for UNIVATION UNICONDYLAR KNEE SYSTEM, Substantially Equivalent on 2008-09-22. Applicant: Aesculap Implant Systems, Inc.. Device class: 2.

Clearance details

Applicant
Aesculap Implant Systems, Inc.
Product code
Code HRY
Device class
Class 2
Regulation
21 CFR 888.3530
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Center Valley, PA, US
Download summary PDFView on FDA.gov ↗

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More clearances from Aesculap Implant Systems, Inc.

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Adverse events under product code HRY

product code HRY
Injury
1,551
Malfunction
2,753
Total
4,304

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K081293

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K081293.

Data sourced from openFDA. This site is unofficial and independent of the FDA.