510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K151083Substantially Equivalent

BioBridge Collagen Matrix

Fibralign Corporation, Union City CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K151083 is the FDA 510(k) clearance record for BioBridge Collagen Matrix, a class II device, cleared for Fibralign Corporation on under FDA product code OWY (Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon). FDA's definition for product code OWY reads: "For reinforcement of soft tissue where weakness exists in tendon repair". FDA records list one 510(k) clearance for Fibralign Corporation. As of , FDA records show no recalls naming K151083.

Clearance record

Decision date
Received
(261 days to decision)
Product code
OWY Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Fibralign Corporation 32930 Alvarado-Niles Rd., Suite 350, Union City CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OWY

Trailing 12 months

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

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