ATEC IOM Accessory Instruments— 510(k) K191723

Substantially Equivalent

Alphatec Spine, Inc.

FDA 510(k) clearance K191723 for ATEC IOM Accessory Instruments, Substantially Equivalent on 2019-10-18. Applicant: Alphatec Spine, Inc..

Clearance details

Applicant: Alphatec Spine, Inc.
Product code: Code PDQ
Advisory panel: Ear, Nose, Throat
Date received: 2019-06-27
Decision date: 2019-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsnad, CA, US

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