510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K870200Substantially Equivalent

Sutter Finger Joint Prosthesis

Sutter Biomedical, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870200 is the FDA 510(k) clearance record for SUTTER FINGER JOINT PROSTHESIS, a class II device, cleared for Sutter Biomedical, Inc. on under FDA product code KYJ (Prosthesis, Finger, Constrained, Polymer). FDA records list 11 510(k) clearances for Sutter Biomedical, Inc., from to . As of , FDA records show no recalls naming K870200.

Clearance record

Decision date
Received
(262 days to decision)
Product code
KYJ Prosthesis, Finger, Constrained, Polymer
Regulation
21 CFR 888.3230
Device class
Class II
Review panel
Orthopedic
Applicant
Sutter Biomedical, Inc. 3940 Ruffin Rd., San Diego CA
Third party review
No

Clearances, product code KYJ

Trailing 12 months

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

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