SMOOTH STAPLE IMPLANT— 510(k) K900433

Unknown

Interphase Implants, Inc.

FDA 510(k) clearance K900433 for SMOOTH STAPLE IMPLANT, Unknown on 1990-11-16. Applicant: Interphase Implants, Inc..

Clearance details

Applicant: Interphase Implants, Inc.
Product code: Code MDL
Advisory panel: Dental
Date received: 1990-01-30
Decision date: 1990-11-16
Decision: Unknown
Clearance type: Traditional
Location: Livonia, MI, US

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