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FDA 510(k)

REBOUND HRDV

K-Number: K083467 · 2009-04-23

ApplicantMinnesota Medical Development, Inc.
Decision Date2009-04-23
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REBOUND HRDV is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Medical Development, Inc.. It received FDA 510(k) clearance on 2009-04-23 under 510(k) number K083467. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REBOUND HRDV?

REBOUND HRDV is a medical device that received FDA 510(k) clearance on 2009-04-23. The listed applicant is Minnesota Medical Development, Inc.. The 510(k) number is K083467.

When did REBOUND HRDV receive FDA 510(k) clearance?

REBOUND HRDV received FDA 510(k) clearance on 2009-04-23, under 510(k) number K083467.

Who is the listed applicant for REBOUND HRDV?

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

What is the FDA product code for REBOUND HRDV?

The FDA product code for REBOUND HRDV is FTL.

Related Clinical Trials

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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Other records listing Minnesota Medical Development, Inc. as applicant

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.

K080393MODIFICATION TO REBOUND HRDK063671REBOUND HRD

Related Devices (Code: FTL)

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.

K253956ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)Sofradim ProductionK253125Parietene™ Flat Sheet MeshMedtronic - Sofradim ProductionK251955Onflex™ MeshDavol Inc., Subsidiary of C. R. Bard, Inc.K251557Bard® Mesh; Bard® Mesh Pre-ShapedDavol, Inc.K250869Parietene™ Macroporous Mesh (PPM5050 )Sofradim ProductionK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedDavol, Inc.

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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