510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935593Substantially Equivalent

Anatomic Proportional Shoulder Aps (Hemi-Shoulder) System

Biodynamic Technologies, Inc., Concord CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935593 is the FDA 510(k) clearance record for ANATOMIC PROPORTIONAL SHOULDER APS (HEMI-SHOULDER) SYSTEM, a class II device, cleared for Biodynamic Technologies, Inc. on under FDA product code HSD (Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented). FDA records list 30 510(k) clearances for Biodynamic Technologies, Inc., from to . As of , FDA records show no recalls naming K935593.

Clearance record

Decision date
Received
(329 days to decision)
Product code
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Regulation
21 CFR 888.3690
Device class
Class II
Review panel
Orthopedic
Applicant
Biodynamic Technologies, Inc. 1000 Burnett Ave., Concord CA
510(k) summary
Summary
Third party review
No

Clearances, product code HSD

Trailing 12 months

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

FDA records show no clearances under product code HSD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HSD, 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