510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K080108Substantially Equivalent

Cortoss Bone Augmentation Material

DSM Biomedical, Inc., Malver PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K080108 is the FDA 510(k) clearance record for CORTOSS BONE AUGMENTATION MATERIAL, a class II device, cleared for Orthovita, Inc. on under FDA product code NDN (Cement, Bone, Vertebroplasty). FDA records list 54 510(k) clearances for DSM Biomedical, Inc., from to . As of , FDA records show 4 recalls naming K080108.

Clearance record

Decision date
Received
(507 days to decision)
Product code
NDN Cement, Bone, Vertebroplasty
Regulation
21 CFR 888.3027
Device class
Class II
Review panel
Orthopedic
Applicant
Orthovita, Inc. 45 Great Valley Pkwy., Malver PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NDN

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