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FDA 510(k)

HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2

K-Number: K091390 · 2009-07-30

ApplicantHdc S.R.L.
Decision Date2009-07-30
Product CodeOAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2 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 2009-07-30 under 510(k) number K091390. The device is classified under product code OAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2?

HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2 is a medical device that received FDA 510(k) clearance on 2009-07-30. The listed applicant is Hdc S.R.L.. The 510(k) number is K091390.

When did HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2 receive FDA 510(k) clearance?

HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2 received FDA 510(k) clearance on 2009-07-30, under 510(k) number K091390.

Who is the listed applicant for HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2?

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 SELF LIGATING SPIDER SCREW, MODEL SLI,SL2?

The FDA product code for HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2 is OAT.

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.

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.

Related Devices (Code: OAT)

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.

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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