METRONIC SOFAMOR DANEK CEMENT RESTRICTOR— 510(k) K011998
UnknownMedtronic Sofamor Danek, Inc.
FDA 510(k) clearance K011998 for METRONIC SOFAMOR DANEK CEMENT RESTRICTOR, Unknown on 2001-07-26. Applicant: Medtronic Sofamor Danek, Inc.. Device class: 2.
Clearance details
- Applicant
- Medtronic Sofamor Danek, Inc.
- Product code
- Code JDK
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Special
- Location
- Memphis, TN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.