DeviceClearance

MODIFICATON TO: ZIMMER PERIARTICULAR LOCKING PLATES AND SCREWS— 510(k) K070906

Substantially Equivalent

Zimmer, Inc.

FDA 510(k) clearance K070906 for MODIFICATON TO: ZIMMER PERIARTICULAR LOCKING PLATES AND SCREWS, Substantially Equivalent on 2007-05-01. Applicant: Zimmer, Inc.. Device class: 2.

Clearance details

Applicant
Zimmer, Inc.
Product code
Code HWC
Device class
Class 2
Regulation
21 CFR 888.3040
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Warsaw, IN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code HWC

product code HWC
Death
20
Injury
15,910
Malfunction
8,192
Other
1
Total
24,123

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 K070906

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 K070906.

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