ZIMMER DTO PIN PRESS INSTRUMENT— 510(k) K101704
Substantially EquivalentZimmer Spine, Inc.
FDA 510(k) clearance K101704 for ZIMMER DTO PIN PRESS INSTRUMENT, Substantially Equivalent on 2010-08-18. 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
- Substantially Equivalent
- Clearance type
- Special
- Location
- Minneapolis, MN, US
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