ZIMMER DTO IMPLANT— 510(k) K071879

Unknown

Zimmer Spine, Inc.

FDA 510(k) clearance K071879 for ZIMMER DTO IMPLANT, Unknown on 2007-10-05. Applicant: Zimmer Spine, Inc..

Clearance details

Applicant: Zimmer Spine, Inc.
Product code: Code NQP
Advisory panel: Orthopedic
Date received: 2007-07-09
Decision date: 2007-10-05
Decision: Unknown
Clearance type: Traditional
Location: Minneapolis, MN, US

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