K863854Substantially Equivalent

P.m.d. Intramedullary Cement Restrictor Plug

Name: K863854 P.m.d. Intramedullary Cement Restrictor Plug
Creator: Precision Medical Devices, Inc.
Published: 1986-11-19
License: https://open.fda.gov/license/

Precision Medical Devices, LLC, Camp Hill PA / Traditional, Substantially Equivalent

FDA source

K863854 is the FDA 510(k) clearance record for P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG, cleared for Precision Medical Devices, Inc. on 1986-11-19. FDA records list 3 510(k) clearances for Precision Medical Devices, Inc., from 1984-02-09 to 1986-11-19. As of 2026-09-10, FDA records show no recalls naming K863854.

Clearance record

Decision date: 1986-11-19
Received: 1986-10-02 (48 days to decision)
Review panel: Unknown
Applicant: Precision Medical Devices, Inc. 1400 Mrket St. Suite 101, Camp Hill PA
Third party review: No