ZIMMER MIS LIGHT— 510(k) K080367
Substantially EquivalentZimmer Spine, Inc.
FDA 510(k) clearance K080367 for ZIMMER MIS LIGHT, Substantially Equivalent on 2008-02-22. Applicant: Zimmer Spine, Inc.. Device class: 2.
Clearance details
- Applicant
- Zimmer Spine, Inc.
- Product code
- Code FST
- Device class
- Class 2
- Regulation
- 21 CFR 878.4580
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
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