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Seaspine, Inc.

FDA 510(k) & PMA Approved Devices — 24 products

Total Devices24
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K231654 NorthStar OCT SystemNKG2023-08-03 View
510(k) K132859 INTEGRA FACET FIXATION SYSTEMMRW2013-11-18 View
510(k) K121924 INTEGRA INTERSPINOUS PROCESS SYSTEMPEK2013-09-04 View
510(k) K130830 INTEGRA LAMINOPLASTY SYSTEMNQW2013-05-09 View
510(k) K122571 MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEMNKB2012-12-12 View
510(k) K112206 CARDIFF ANTERIOR CERVICAL PLATE SYSTEMKWQ2012-01-25 View
510(k) K111671 SEASPINE MONOPOLAR PROBE SYSYEMETN2011-12-28 View
510(k) K102026 SEASPINE SPACER SYSTEMMAX2011-05-12 View
510(k) K103297 REDONDO-LMAX2011-01-27 View
510(k) K092521 ZUMA-COVE2010-04-13 View
510(k) K082309 CAMBRIAODP2009-04-09 View
510(k) K083338 CARDIFF ANTERIOR CERVICAL PLATE SYSTEMKWQ2009-02-02 View
510(k) K083089 NEWPORT SPINAL SYSTEMNKB2009-01-13 View
510(k) K082926 ZUMA, MODEL 55-XXXX/56-XXXXOVD2008-12-22 View
510(k) K082310 HOLLYWOOD, PACIFICA, REDONDO, VENTURAMAX2008-11-10 View
510(k) K072729 SIERRAKWP2008-04-17 View
510(k) K080526 SIERRA SYSTEMKWP2008-04-16 View
510(k) K072605 MALIBU SPINAL SYSTEMNKB2007-12-20 View
510(k) K071726 ZUMAMQP2007-10-23 View
510(k) K062934 SIERRAMNI2006-11-16 View
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