MODIFIED E-PACK PROCEDURE KIT

K970317 · ETHICON, Inc. · GAM · Apr 25, 1997 · General, Plastic Surgery

Device Facts

Record IDK970317
Device NameMODIFIED E-PACK PROCEDURE KIT
ApplicantETHICON, Inc.
Product CodeGAM · General, Plastic Surgery
Decision DateApr 25, 1997
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 878.4493
Device ClassClass 2

Indications for Use

There is no change in the approved intended use of the device when provided in the procedure kit

Device Story

E-PACK Procedural Kit; collection of legally marketed individual medical devices manufactured by or for ETHICON, Inc.; packaged together in thermoformed blister tray or sealed pouch for surgeon convenience; intended for use in surgical procedures; components retain original approved indications; sterilization via ethylene oxide.

Clinical Evidence

No clinical data; bench testing only.

Technological Characteristics

Kit containing legally marketed individual medical devices; sterilization via ethylene oxide (SAL 10^-6); packaging in thermoformed blister tray or flexible sealed pouch.

Regulatory Classification

Identification

An absorbable poly(glycolide/l-lactide) surgical suture (PGL suture) is an absorbable sterile, flexible strand as prepared and synthesized from homopolymers of glycolide and copolymers made from 90 percent glycolide and 10 percent l-lactide, and is indicated for use in soft tissue approximation. A PGL suture meets United States Pharmacopeia (U.S.P.) requirements as described in the U.S.P. “Monograph for Absorbable Surgical Sutures;” it may be monofilament or multifilament (braided) in form; it may be uncoated or coated; and it may be undyed or dyed with an FDA-approved color additive. Also, the suture may be provided with or without a standard needle attached.

Special Controls

*Classification.* Class II (special controls). The special control for this device is FDA's “Class II Special Controls Guidance Document: Surgical Sutures; Guidance for Industry and FDA.” See § 878.1(e) for the availability of this guidance document.

Predicate Devices

Submission Summary (Full Text)

{0} APR 25 1997 K970317 # SECTION 7 ## SUMMARY OF SAFETY AND EFFECTIVENESS ### 510(k) Summary of Safety and Effectiveness Information supporting claims of substantial equivalence, as defined under the Federal Food, Drug and Cosmetic Act, respecting safety and effectiveness is summarized below. For the convenience of the Reviewer, this summary is formatted in accordance with the Agency's final rule "...510(k) Summaries and 510(k) Statements..." (21 CFR 807) and can be used to provide a substantial equivalence summary to anyone requesting it from the Agency. **MODIFIED DEVICE NAME:** E-PACK Procedural Kit **PREDICATE DEVICE NAME:** Predicate Device E-PACK Procedural Kit ### 510(k) SUMMARY #### Device Description All components of E-PACK procedural kit are legally marketed devices manufactured by or for ETHICON, Inc. and labeled for approved uses. These products are packaged together in the form of a "kit" for the convenience of the surgeon. #### Intended Use There is no change in the approved intended use of the device when provided in the procedure kit Continued on next page Modified E-PACK Procedure Kit ETHICON, Inc. {1} SUMMARY OF SAFETY AND EFFECTIVENESS, Continued 510(k) SUMMARY, Continued Sterilization E-Pack procedural kits are sterilized by ethylene oxide for minimum sterility level of 10/6. Packaging The component devices in the E-PACK procedure kit may be packaged in their current individual package or paper folders into one large thermoformed blister tray or in a flexible configuration consisting of a sealed pouch. Conclusions Based on the 510(k) summaries and 510(k) statements (21 CFR 807) and the information provided herein, we conclude that the new device is substantially equivalent to the Predicate Device under the Federal Food, Drug, and Cosmetic Act. Contact John D. Paulson, Ph.D. Vice President, Regulatory Affairs and Quality Assurance ETHICON, Inc. Rt. #22, West Somerville, NJ 08876-0151 Date January 24, 1997 Modified E-PACK Procedure Kit ETHICON, Inc.
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