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
K950009Substantially Equivalent

Powergrip(tm) Compression Fixation Device

Synvasive Technology, Inc., Rancho Cordova CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950009 is the FDA 510(k) clearance record for POWERGRIP(TM) COMPRESSION FIXATION DEVICE, a class II device, cleared for Synvasive Technology, Inc. on under FDA product code JDW (Pin, Fixation, Threaded). FDA records list 10 510(k) clearances for Synvasive Technology, Inc., from to . As of , FDA records show no recalls naming K950009.

Clearance record

Decision date
Received
(227 days to decision)
Product code
JDW Pin, Fixation, Threaded
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
Synvasive Technology, Inc. 11328 Sunrise Gold Cir., Rancho Cordova CA
510(k) summary
Statement
Third party review
No

Clearances, product code JDW

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