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FDA 510(k)

CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR

K-Number: K090835 · 2009-06-22

ApplicantLinvatec Corp.
Decision Date2009-06-22
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 2009-06-22 under 510(k) number K090835. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR?

CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR is a medical device that received FDA 510(k) clearance on 2009-06-22. The listed applicant is Linvatec Corp.. The 510(k) number is K090835.

When did CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR receive FDA 510(k) clearance?

CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR received FDA 510(k) clearance on 2009-06-22, under 510(k) number K090835.

Who is the listed applicant for CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR?

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

What is the FDA product code for CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR?

The FDA product code for CONMED LINVATEC BIO MINI-REVO SUTURE ANCHOR, MODEL C6170CR is MAI.

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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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