Atlas FDA

FIXATION STAPLE KIT - DLIDE HAMMER

FDA 510(k) clearance K834515 · decided 1984-04-23

Clearance details

K-number
K834515
Device name
FIXATION STAPLE KIT - DLIDE HAMMER
Applicant
Stryker Corp.
Decision
Substantially Equivalent
Date received
1983-12-21
Decision date
1984-04-23
Days to decision
124 days
Clearance type
Traditional
Product code
HXJ
Device class
1
Regulation number
888.4540
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
IN-TAC BONE ANCHOR SYSTEM (K964953)Influence, Inc.1997-02-13
UROTAC BONE ANCHOR INSERTER (K962372)Influence, Inc.1996-08-19
ELECTRIC WIRE DRIVER, MODEL 2640E (K930205)Micro Surgical Instruments Corp.1993-08-02
OSTEOTOMY BONE STAPLE (K830255)Techmedica, Inc.1983-03-09
STAPLE INSERTER-EXTRACTOR FOR ARTHROS (K830456)Instrument Makar, Inc.1983-03-09

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
VITAGEL RT3 SUTGICAL HEMOSTAT (P050044/S033)Stryker Corp.2017-03-02
VITAGEL RT3 SURGICAL HEMOSTAT (P050044/S032)Stryker Corp.2015-07-16
VITAGEL SURGICAL HEMOSTAT (RT3) (P050044/S031)Stryker Corp.2015-04-14
VITAGEL SURGICAL HEMOSTAT (RT3) (P050044/S030)Stryker Corp.2015-04-13
VITAGEL RT3 SURGICAL HEMOSTAT (P050044/S029)Stryker Corp.2014-12-12
VITAGEL RT3 DELIVERY SYSTEM (P050044/S028)Stryker Corp.2014-06-05
VITAGEL SURGICAL HEMOSTAT (VITAGEL) (P050044/S026)Stryker Corp.2014-02-11
RT3 SURGICAL HEMOSTAT (P050044/S027)Stryker Corp.2014-01-27