MERLIN SPINE SYSTEM— 510(k) K033901

Substantially Equivalent

Depuy Spine, Inc.

FDA 510(k) clearance K033901 for MERLIN SPINE SYSTEM, Substantially Equivalent on 2004-03-31. Applicant: Depuy Spine, Inc.. Device class: 2.

Clearance details

Applicant
Depuy Spine, Inc.
Product code
Code NKB
Device class
Class 2
Regulation
21 CFR 888.3070
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Raynham, MA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code NKB

product code NKB
Death
27
Injury
5,033
Malfunction
4,140
Total
9,200

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 →

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