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
K222220Substantially Equivalent

SpinMedix Absorbable Fibrous Membrane

Celestray Biotech Company, LLC., Bethesda MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222220 is the FDA 510(k) clearance record for SpinMedix Absorbable Fibrous Membrane, a class II device, cleared for Celestray Biotech Company, LLC., on under FDA product code OWW (Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon). FDA's definition for product code OWW reads: "For reinforcement of soft tissue where weakness exists during tendon repair procedures". FDA records list 2 510(k) clearances for Celestray Biotech Company, LLC.,, from to . As of , FDA records show no recalls naming K222220.

Clearance record

Decision date
Received
(346 days to decision)
Product code
OWW Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Celestray Biotech Company, LLC., P.O. Box 341754, Bethesda MD
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OWW

Trailing 12 months

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

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