ZIMMER DTO IMPLANT— 510(k) K071879
UnknownZimmer Spine, Inc.
FDA 510(k) clearance K071879 for ZIMMER DTO IMPLANT, Unknown on 2007-10-05. Applicant: Zimmer Spine, Inc.. Device class: 2.
Clearance details
- Applicant
- Zimmer Spine, Inc.
- Product code
- Code NQP
- 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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Recalls naming K071879
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K071879.
Data sourced from openFDA. This site is unofficial and independent of the FDA.