510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K091087Substantially Equivalent

Modification to V-Loc 180 Absorbable Wound Closure Device

Surgical Devices, Tyco Healthcare Group LP, North Haven CT / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K091087 is the FDA 510(k) clearance record for MODIFICATION TO V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE, a class II device, cleared for Surgical Devices, Tyco Healthcare Group LP on under FDA product code GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid). FDA records list 2 510(k) clearances for Surgical Devices, Tyco Healthcare Group LP, from to . As of , FDA records show one recall naming K091087.

Clearance record

Decision date
Received
(7 days to decision)
Product code
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid
Regulation
21 CFR 878.4493
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Surgical Devices, Tyco Healthcare Group LP 60 Middletown Ave., North Haven CT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GAM

Trailing 12 months
5 clearances under product code GAM in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code GAM, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260