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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K101255

ALPHATEC SPINE ANTERIOR LUMBAR PLATING SYSTEM · Alphatec Spine, Inc. · decided 2010-07-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Aspida51001-16ALPHATEC SPINE, INC.KWQ00844856062931
Aspida51001-12ALPHATEC SPINE, INC.KWQ00844856062917
Aspida51002-18ALPHATEC SPINE, INC.KWQ00844856063006
Aspida51001-14ALPHATEC SPINE, INC.KWQ00844856062924
Aspida51070-25ALPHATEC SPINE, INC.KWQ00844856063037
Aspida51002-08ALPHATEC SPINE, INC.KWQ00844856062955
Aspida51060-30ALPHATEC SPINE, INC.KWQ00844856036956
Aspida51060-35ALPHATEC SPINE, INC.KWQ00844856063020
Aspida51002-16ALPHATEC SPINE, INC.KWQ00844856062993
Aspida51001-08ALPHATEC SPINE, INC.KWQ00844856062894
Aspida51002-14ALPHATEC SPINE, INC.KWQ00844856062986
Aspida51070-35ALPHATEC SPINE, INC.KWQ00844856063044
Aspida51070-30ALPHATEC SPINE, INC.KWQ00844856037021
Aspida51001-10ALPHATEC SPINE, INC.KWQ00844856062900
Aspida51001-18ALPHATEC SPINE, INC.KWQ00844856062948
Aspida51002-12ALPHATEC SPINE, INC.KWQ00844856062979
Aspida51002-10ALPHATEC SPINE, INC.KWQ00844856062962
Aspida51060-25ALPHATEC SPINE, INC.KWQ00844856063013