FDA.reportPublic FDA data

NEXT ORTHOSURGICAL

Matched from indexed company URL: Next OrthoSurgical

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30100207543010020754NEXT ORTHOSURGICAL1N2020-04-253270 Corporate Vw Ste A Vista CA US 92081

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00840314114310Nex-D2 - FIXED SCREW, 4.0MM X 20MM760-295-3600Info@nextorthosurgical.com
00840314115560Nex-D2 - CANNULATED POLYAXIAL SCREW, 5.0MM X 20MM760-295-3600Info@nextorthosurgical.com
00840314116567Nex-D2 - SET SCREW, T-30 HEXALOBE760-295-3600Info@nextorthosurgical.com
00840314116574Nex-D2 - SET SCREW, CANNULATED, T-30 HEXALOBE760-295-3600Info@nextorthosurgical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1519571293394789K190981NEX-D2 Posterior Fixation SystemNKB2020-01-15
1519571644857436K161608InterForm Cervical Interbody Cage SystemODP2016-09-30
1519571290360656K161499VertiForm Posterior Fixation SystemNKB2016-07-29
1519571991528422K141291VERTIFORM POSTERIOR FIXATION SYSTEMNKB2014-08-26
1519571274313819K131540INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICEMAX2013-09-03
1519571312137816K131082INTERFORM INTERBODY CAGE SYSTEMMAX2013-08-26
1519571187846721K110045INTERFUSE DA INVERTEBRAL BODY FUSION DEVICEMAX2011-02-03
1519571265962721K102277INTERFUSE T INVERTEBRAL BODY FUSION DEVICEMAX2010-10-06
1519571724757041K080673INTERFUSE INTERVERTEBRAL BODY FUSION DEVICEMAX2008-06-10
1519571484198016
1519571916821157
1519572037326006

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MAX52013-09-03
NKB32020-01-15
ODP12016-09-30

PMN#

GUDID#

80 records. Showing 1-40. Next