510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K132910Substantially Equivalent

Depuy Synthes Spine Dens Access System

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

K132910 is the FDA 510(k) clearance record for DEPUY SYNTHES SPINE DENS ACCESS SYSTEM, a class II device, cleared for Synthes USA Products, LLC on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 479 510(k) clearances for Synthes USA Products, LLC, from to . As of , FDA records show no recalls naming K132910.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Synthes USA Products, LLC 1302 Wrights Ln. E., West Chester PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HWC

Trailing 12 months
23 clearances under product code HWC in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code HWC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20263
May 20264
June 20262
July 20261
August 20263
September 20264
October 20262