510(k) K063769

Device
ALPHA BIO BONE FIXATION SCREW SYSTEM
Applicant
ALPHA-BIO TEC LTD
510(k) number
K063769
Product code
DZL  
Decision
Substantially Equivalent (SESE)
Decision date
2007-03-30
Date received
2006-12-20
Regulation
872.4880
Classification name
Screw, Fixation, Intraosseous
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
DANIEL J MANELLI
Address
5335 Wisconsin Ave. NW Suite 440 Washington DC US 20015 20015

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code DZL  

510(k)DeviceApplicantDecision date
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K251569Bone ScrewOsstem Implant Co., Ltd.2025-08-13
K243190USTOMED Bone Fixation/Bone Augmentation Systems - PINUstomed Instrumente Ulrich Storz GmbH & Co. KG2025-06-27
K233419GBR SystemProimtech Saglik Urunleri Anonim Sirketi2025-01-03
K240321MP Pin flat without thread (36BMP000020/MP20)Hager& Meisinger GmbH2024-10-17
K233721KLS Martin Drill-Free MMF ScrewKLS-Martin L.P.2024-09-17
K231599Stryker MP, Mandible, HMMF and MMF AXS ScrewsStryker Leibinger GmbH & Co KG2023-08-24
K222367SAVE GBRDentis Co., Ltd.2023-03-23
K201210The Micro Screw System, Micro Screw System BasicHager& Meisinger GmbH2021-10-08
K201561Membrane Screws and Membrane TacksNeoss Limited2020-10-05
K182881Bone Screw, Bone TackOsstem Implant Co., Ltd.2019-08-09
K181854OssBuilder SystemOsstem Implant Co., Ltd.2019-05-07
K171831Intra-Lock Bone Fixation SystemIntra-Lock International, Inc.2017-10-26
K161857Salvin Tenting Screw SystemSalvin Dental Specialties2017-04-28
K160991Neo GBR SystemNeobiotech Co., Ltd.2017-01-10

Legacy Summary

summary

FDA Review

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