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FDA 510(k)

BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS

K-Number: K032700 · 2003-10-09

ApplicantBlackstone Medical, Inc.
Decision Date2003-10-09
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS is the device name listed in this FDA 510(k) record. The listed applicant is Blackstone Medical, Inc.. It received FDA 510(k) clearance on 2003-10-09 under 510(k) number K032700. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS?

BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS is a medical device that received FDA 510(k) clearance on 2003-10-09. The listed applicant is Blackstone Medical, Inc.. The 510(k) number is K032700.

When did BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS receive FDA 510(k) clearance?

BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS received FDA 510(k) clearance on 2003-10-09, under 510(k) number K032700.

Who is the listed applicant for BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS?

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

What is the FDA product code for BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS?

The FDA product code for BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS is MQP.

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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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