Optima ZS Transition Screw— 510(k) K071880
UnknownZimmer Spine, Inc.
FDA 510(k) clearance K071880 for Optima ZS Transition Screw, Unknown on 2007-10-05. Applicant: Zimmer Spine, Inc.. Device class: 2.
Clearance details
- Applicant
- Zimmer Spine, Inc.
- Product code
- Code MNI
- Device class
- Class 2
- Regulation
- 21 CFR 888.3070
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
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Adverse events under product code MNI
product code MNI- Injury
- 641
- Total
- 641
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.