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FDA 510(k)

SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01

K-Number: K090530 · 2009-05-20

ApplicantRoss Creek Medical, Inc.
Decision Date2009-05-20
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01 is the device name listed in this FDA 510(k) record. The listed applicant is Ross Creek Medical, Inc.. It received FDA 510(k) clearance on 2009-05-20 under 510(k) number K090530. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01?

SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01 is a medical device that received FDA 510(k) clearance on 2009-05-20. The listed applicant is Ross Creek Medical, Inc.. The 510(k) number is K090530.

When did SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01 receive FDA 510(k) clearance?

SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01 received FDA 510(k) clearance on 2009-05-20, under 510(k) number K090530.

Who is the listed applicant for SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01?

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

What is the FDA product code for SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01?

The FDA product code for SPIN-LOC SUTURE ANCHOR SYSTEM FG-0302-01,FG-0305-01 is MBI.

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Related Devices (Code: MBI)

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.

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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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