Atlas FDA

HENNING MENISCAL SUTURE KIT

FDA 510(k) clearance K843942 · decided 1985-04-15

Clearance details

K-number
K843942
Device name
HENNING MENISCAL SUTURE KIT
Applicant
Stryker Corp.
Decision
Substantially Equivalent
Date received
1984-10-09
Decision date
1985-04-15
Days to decision
188 days
Clearance type
Traditional
Product code
LXH
Device class
1
Regulation number
888.4540
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Kalamazoo, MI, 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.

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MICROPERFORATION INSTRUMENT (K001507)Smith & Nephew, Inc.2000-06-14
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ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY (K943873)Orthomet, Inc.1995-04-26
SPINAL MARKER (K944188)Leibinger L.P.1995-04-13
STEADMAN LIGAMENT GRAFT PASSER AND PROTECTOR (K941896)Depuy, Inc.1994-11-07
HYPERFLEX FLEXIBLE GUIDEWIRES (K941711)Linvatec Corp.1994-08-26
STRYKER FEMORAL CANAL BRUSH, ACETABULAR BRUSH (K941605)Stryker Corp.1994-08-05
PUNCH SURGICAL (K933772)Mahe-Medizintechnik1994-02-01
SOFAMOR ORTHOPAEDIC INSTRUMENTS (K933242)Danek Medical, Inc.1994-01-28

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