510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890902Substantially Equivalent

Biofix* Biodegradable Fixation Rod

Davis & Geck, Inc., Danbury CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890902 is the FDA 510(k) clearance record for BIOFIX* BIODEGRADABLE FIXATION ROD, a class II device, cleared for Davis & Geck, Inc. on under FDA product code HTY (Pin, Fixation, Smooth). FDA records list 45 510(k) clearances for Davis & Geck, Inc., from to . As of , FDA records show no recalls naming K890902.

Clearance record

Decision date
Received
(254 days to decision)
Product code
HTY Pin, Fixation, Smooth
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Davis & Geck, Inc. American Cynamid Company, Danbury CT
Third party review
No

Clearances, product code HTY

Trailing 12 months
2 clearances under product code HTY in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HTY, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260