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FDA 510(k)

RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS

K-Number: K881757 · 1988-07-15

ApplicantDowns Surgical , Ltd.
Decision Date1988-07-15
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1988-07-15 under 510(k) number K881757. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS?

RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS is a medical device that received FDA 510(k) clearance on 1988-07-15. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K881757.

When did RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS receive FDA 510(k) clearance?

RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS received FDA 510(k) clearance on 1988-07-15, under 510(k) number K881757.

Who is the listed applicant for RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS?

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

What is the FDA product code for RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS?

The FDA product code for RESUBMITTED JUNIPER T.M. JOINT DISTRACTION FORCEPS is ETN.

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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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