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FDA 510(k)

SMALL BONE WEDGE

K-Number: K070592 · 2007-10-05

ApplicantWrightmedicaltechnologyinc
Decision Date2007-10-05
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMALL BONE WEDGE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K070592. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMALL BONE WEDGE?

SMALL BONE WEDGE is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K070592.

When did SMALL BONE WEDGE receive FDA 510(k) clearance?

SMALL BONE WEDGE received FDA 510(k) clearance on 2007-10-05, under 510(k) number K070592.

Who is the listed applicant for SMALL BONE WEDGE?

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

What is the FDA product code for SMALL BONE WEDGE?

The FDA product code for SMALL BONE WEDGE is HRS.

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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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