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FDA 510(k)

BIOPRO MEMORY STAPLE

K-Number: K061798 · 2006-08-21

ApplicantBiopro, Inc.
Decision Date2006-08-21
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOPRO MEMORY STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Biopro, Inc.. It received FDA 510(k) clearance on 2006-08-21 under 510(k) number K061798. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPRO MEMORY STAPLE?

BIOPRO MEMORY STAPLE is a medical device that received FDA 510(k) clearance on 2006-08-21. The listed applicant is Biopro, Inc.. The 510(k) number is K061798.

When did BIOPRO MEMORY STAPLE receive FDA 510(k) clearance?

BIOPRO MEMORY STAPLE received FDA 510(k) clearance on 2006-08-21, under 510(k) number K061798.

Who is the listed applicant for BIOPRO MEMORY STAPLE?

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

What is the FDA product code for BIOPRO MEMORY STAPLE?

The FDA product code for BIOPRO MEMORY STAPLE is JDR.

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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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