510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883065Substantially Equivalent

Alloprep System

Osteotech Inc, Shrewsbury NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883065 is the FDA 510(k) clearance record for ALLOPREP SYSTEM, a class I device, cleared for Osteotech, Inc. on under FDA product code KIT (Media And Components, Synthetic Cell And Tissue Culture). FDA records list 24 510(k) clearances for Osteotech, Inc., from to . As of , FDA records show no recalls naming K883065.

Clearance record

Decision date
Received
(85 days to decision)
Product code
KIT Media And Components, Synthetic Cell And Tissue Culture
Regulation
21 CFR 864.2220
Device class
Class I
Review panel
Hematology
Applicant
Osteotech, Inc. 1151 E Sherewsbury Ave., Shrewsbury NJ
Third party review
No

Clearances, product code KIT

Trailing 12 months

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

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