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FDA 510(k)

HDC STERILE SPIDER SCREW

K-Number: K071851 · 2007-10-18

ApplicantHdc S.R.L.
Decision Date2007-10-18
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HDC STERILE SPIDER SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Hdc S.R.L.. It received FDA 510(k) clearance on 2007-10-18 under 510(k) number K071851. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HDC STERILE SPIDER SCREW?

HDC STERILE SPIDER SCREW is a medical device that received FDA 510(k) clearance on 2007-10-18. The listed applicant is Hdc S.R.L.. The 510(k) number is K071851.

When did HDC STERILE SPIDER SCREW receive FDA 510(k) clearance?

HDC STERILE SPIDER SCREW received FDA 510(k) clearance on 2007-10-18, under 510(k) number K071851.

Who is the listed applicant for HDC STERILE SPIDER SCREW?

The FDA 510(k) record lists Hdc S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HDC STERILE SPIDER SCREW?

The FDA product code for HDC STERILE SPIDER SCREW is DZE.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Hdc S.R.L. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K091390HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2K052471HDC SPIDER SCREW

Related Devices (Code: DZE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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