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FDA 510(k)

MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR

K-Number: K010479 · 2001-05-08

ApplicantBonutti Research, Inc.
Decision Date2001-05-08
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Bonutti Research, Inc.. It received FDA 510(k) clearance on 2001-05-08 under 510(k) number K010479. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR?

MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR is a medical device that received FDA 510(k) clearance on 2001-05-08. The listed applicant is Bonutti Research, Inc.. The 510(k) number is K010479.

When did MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR receive FDA 510(k) clearance?

MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR received FDA 510(k) clearance on 2001-05-08, under 510(k) number K010479.

Who is the listed applicant for MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR?

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

What is the FDA product code for MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR?

The FDA product code for MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR is HTY.

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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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