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FDA 510(k)

LACTOSORB POP RIVET

K-Number: K951658 · 1995-07-25

ApplicantPoly-Medics,Inc.
Decision Date1995-07-25
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

LACTOSORB POP RIVET is the device name listed in this FDA 510(k) record. The listed applicant is Poly-Medics,Inc.. It received FDA 510(k) clearance on 1995-07-25 under 510(k) number K951658. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the LACTOSORB POP RIVET?

LACTOSORB POP RIVET is a medical device that received FDA 510(k) clearance on 1995-07-25. The listed applicant is Poly-Medics,Inc.. The 510(k) number is K951658.

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

LACTOSORB POP RIVET received FDA 510(k) clearance on 1995-07-25, under 510(k) number K951658.

Who is the listed applicant for LACTOSORB POP RIVET?

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

What is the FDA product code for LACTOSORB POP RIVET?

The FDA product code for LACTOSORB POP RIVET is JDR.

Related Clinical Trials

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Other records listing Poly-Medics,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.

K960988LACTOSORB TRAUMA PLATING SYSTEMK955729LACTOSORB TRAUMA PLATING SYSTEMK954443LACTOSORB SUTURE ANCHORK934861HARD TISSUE REPLACEMENT (HTR) GRANULAR

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Official Source

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