PDS PLUS ANTIBACTERIAL SUTURE— 510(k) K061037

Substantially Equivalent

ETHICON, Inc.

FDA 510(k) clearance K061037 for PDS PLUS ANTIBACTERIAL SUTURE, Substantially Equivalent on 2006-07-14. Applicant: ETHICON, Inc.. Device class: 2.

Clearance details

Applicant
ETHICON, Inc.
Product code
Code NEW
Device class
Class 2
Regulation
21 CFR 878.4840
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Somerville, NJ, US
Download summary PDFView on FDA.gov ↗

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More clearances from ETHICON, Inc.

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Adverse events under product code NEW

product code NEW
Death
32
Injury
2,179
Malfunction
8,975
Total
11,186

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 K061037

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 K061037.

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