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FDA 510(k)

AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW

K-Number: K120148 · 2012-10-02

ApplicantAdvanced Orthopaedic Solutions, Inc.
Decision Date2012-10-02
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Orthopaedic Solutions, Inc.. It received FDA 510(k) clearance on 2012-10-02 under 510(k) number K120148. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW?

AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW is a medical device that received FDA 510(k) clearance on 2012-10-02. The listed applicant is Advanced Orthopaedic Solutions, Inc.. The 510(k) number is K120148.

When did AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW receive FDA 510(k) clearance?

AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW received FDA 510(k) clearance on 2012-10-02, under 510(k) number K120148.

Who is the listed applicant for AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW?

The FDA 510(k) record lists Advanced Orthopaedic Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW?

The FDA product code for AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREW is HSB.

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Official Source

View on FDA Database →

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

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