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FDA 510(k)

SURGICAL DYNAMICS POP RIVET

K-Number: K961585 · 1996-07-10

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1996-07-10
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SURGICAL DYNAMICS POP RIVET is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1996-07-10 under 510(k) number K961585. 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 SURGICAL DYNAMICS POP RIVET?

SURGICAL DYNAMICS POP RIVET is a medical device that received FDA 510(k) clearance on 1996-07-10. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K961585.

When did SURGICAL DYNAMICS POP RIVET receive FDA 510(k) clearance?

SURGICAL DYNAMICS POP RIVET received FDA 510(k) clearance on 1996-07-10, under 510(k) number K961585.

Who is the listed applicant for SURGICAL DYNAMICS POP RIVET?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL DYNAMICS POP RIVET?

The FDA product code for SURGICAL DYNAMICS POP RIVET 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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