← Back to catalogue

BARD PERMAFIX FIXATION SYSTEM - 0113016

FDA 510(k)

Class II (US FDA 510(k))

510(k) K092483

by C. R. Bard, Inc.

Identifiers

510(k) Number
K092483 FDA 510(k)
FDA Product Code
GDW FDA 510(k)
Models / Variants
0113012 FDA 510(k)
0113014 FDA 510(k)
0113016 FDA 510(k)
0116018 FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4750 FDA 510(k)
Regulation Number
878.4750 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

BARD PERMAFIX FIXATION SYSTEM - 0113016 by C. R. Bard, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 4 models — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
C. R. Bard, Inc.
FDA Applicant
C.R. Bard, Inc.

Sources (1)

  • FDA 510(k) K092483 24 fields · synced Jun 18, 2026