SYNTHES SYNMESH SPACER SYSTEM— 510(k) K003275

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K003275 for SYNTHES SYNMESH SPACER SYSTEM, Substantially Equivalent on 2001-04-23. Applicant: Synthes (Usa). Device class: 2.

Clearance details

Applicant
Synthes (Usa)
Product code
Code MQP
Device class
Class 2
Regulation
21 CFR 888.3060
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Paoli, PA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MQP

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More clearances from Synthes (Usa)

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Adverse events under product code MQP

product code MQP
Injury
372
Malfunction
519
Total
891

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 K003275

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 K003275.

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