Cleared Traditional

K873274 - PLASTER TABLE 1418
(FDA 510(k) Clearance)

K873274 · Stierlen-Maquet AG · General & Plastic Surgery

Sep 1987

Decision

31d

Days

Class 1

Risk

K873274 is an FDA 510(k) clearance for the PLASTER TABLE 1418, a Table, Surgical With Orthopedic Accessories, Manual (Class I — General Controls, product code JEB), submitted by Stierlen-Maquet AG (West Germany, GR). The FDA issued a Cleared decision on September 17, 1987, 31 days after receiving the submission on August 17, 1987. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4950.

Submission Details

510(k) Number	K873274 FDA.gov
FDA Decision	Cleared SESE
Date Received	August 17, 1987
Decision Date	September 17, 1987
Days to Decision	31 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—