510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K870842Substantially Equivalent

Schultz Phalangeal Comp Rasp/metacarpal Comp Rasp

Warsaw Orthopedic, Inc., Warsaw IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870842 is the FDA 510(k) clearance record for SCHULTZ PHALANGEAL COMP RASP/METACARPAL COMP RASP, a class I device, cleared for Warsaw Orthopedic, Inc. on under FDA product code HTP (File). FDA records list 24 510(k) clearances for Warsaw Orthopedic, Inc., from to . As of , FDA records show no recalls naming K870842.

Clearance record

Decision date
Received
(85 days to decision)
Product code
HTP File
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Applicant
Warsaw Orthopedic, Inc. P.O. Box 1157, Warsaw IN
Third party review
No

Clearances, product code HTP

Trailing 12 months

FDA records hold no clearances under product code HTP in the trailing twelve months.

FDA records show no clearances under product code HTP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HTP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260