510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K112085Substantially Equivalent

Synthes Lcp Pediatric Plate Systems

Synthes (USA) Products LLC, West Chester PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K112085 is the FDA 510(k) clearance record for SYNTHES LCP PEDIATRIC PLATE SYSTEMS, a class II device, cleared for Synthes (USA) Products, LLC on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 479 510(k) clearances for Synthes (USA) Products, LLC, from to . As of , FDA records show no recalls naming K112085.

Clearance record

Decision date
Received
(119 days to decision)
Product code
HRS Plate, Fixation, Bone
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Synthes (USA) Products, LLC 1301 Goshen Pkwy., West Chester PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HRS

Trailing 12 months
55 clearances under product code HRS in the twelve months to November 2026, March 2026 the highest month at 13.
Show the numbers
Monthly 510(k) clearances under FDA product code HRS, trailing twelve months
MonthClearances
December 20255
January 20264
February 20265
March 202613
April 20266
May 20262
June 20265
July 20265
August 20263
September 20265
October 20262
November 20260