INTERMEDULLARY BRUSH— 510(k) K771016

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K771016 for INTERMEDULLARY BRUSH, Substantially Equivalent on 1978-01-12. Applicant: Howmedica Corp.. Device class: 1.

Clearance details

Applicant: Howmedica Corp.
Product code: Code HTR
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1977-06-06
Decision date: 1978-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HTR

K870329 — ACETABULAR BRUSH #1202 & FEMORAL CON. BRUSH #12021987-02-13
K870333 — BIODYNAMICS SMALL JOINT BRUSH #12031987-02-13
K870349 — BIODYNAMICS FEMORAL CANAL BRUSH #12011987-02-13
K813093 — RICHARDS ACETABULAR BRUSH1981-11-20
K812506 — THE ARTHROFILE1981-09-24

More clearances from Howmedica Corp.

K983528 — MICRO DYNAMIC MESH1998-12-23
K983404 — TYPE 3 FEMORAL COMPONENTS1998-12-22
K980925 — DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION1998-12-16
K980926 — DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION1998-12-16
K980626 — DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION1998-12-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.